Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 032, 47712-47714 [2013-19020]

Download as PDF 47712 Federal Register / Vol. 78, No. 151 / Tuesday, August 6, 2013 / Notices recognized consensus standards, as needed, in the Federal Register once a year, or more often, if necessary. Beginning with Recognition List Number: 033, FDA will no longer be announcing minor revisions to the list of recognized consensus standards such as technical contact person, relevant guidance, processes affected, CFR citations, and product codes. tkelley on DSK3SPTVN1PROD with NOTICES V. Recommendation of Standards for Recognition by FDA Any person may recommend consensus standards as candidates for recognition under section 514 of the FD&C Act by submitting such recommendations, with reasons for the recommendation, to the contact person (see FOR FURTHER INFORMATION CONTACT). To be properly considered, such recommendations should contain, at a minimum, the following information: (1) Title of the standard; (2) any reference number and date; (3) name and address of the national or international standards development organization; (4) a proposed list of devices for which a declaration of conformity to this standard should routinely apply; and (5) a brief identification of the testing or performance or other characteristics of the device(s) that would be addressed by a declaration of conformity. VI. Electronic Access You may obtain a copy of ‘‘Guidance on the Recognition and Use of Consensus Standards’’ by using the Internet. The Center for Devices and Radiological Health (CDRH) maintains a site on the Internet for easy access to information including text, graphics, and files that you may download to a personal computer with access to the Internet. Updated on a regular basis, the CDRH home page includes the guidance as well as the current list of recognized standards and other standards-related documents. After publication in the Federal Register, this notice announcing ‘‘Modification to the List of Recognized Standards, Recognition List Number: 031’’ will be available on the CDRH home page. You may access the CDRH home page at https://www.fda.gov/ MedicalDevices. You may access ‘‘Guidance on the Recognition and Use of Consensus Standards,’’ and the searchable database for ‘‘FDA Recognized Consensus Standards’’ at https://www.fda.gov/ MedicalDevices/ DeviceRegulationandGuidance/ Standards. This Federal Register document on modifications in FDA’s recognition of consensus standards is available at VerDate Mar<15>2010 19:47 Aug 05, 2013 Jkt 229001 https://www.fda.gov/MedicalDevices/ DeviceRegulationandGuidance/ Standards/ucm123792.htm. VII. Submission of Comments and Effective Date Interested persons may submit to the contact person (see FOR FURTHER INFORMATION CONTACT) either electronic or written comments regarding this document. It is only necessary to send one set of comments. Comments are to be identified with the docket number found in brackets in the heading of this document. FDA will consider any comments received in determining whether to amend the current listing of modifications to the list of recognized standards, Recognition List Number: 031. These modifications to the list of recognized standards are effective upon publication of this notice in the Federal Register. Dated: July 31, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013–19019 Filed 8–5–13; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2004–N–0451] (formerly 2004N–0226) Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 032 AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing a publication containing modifications the Agency is making to the list of standards FDA recognizes for use in premarket reviews (FDA recognized consensus standards). Specifically, this publication announces the addition of a list of recognized standards that are relevant to interoperability of medical devices. This publication, entitled ‘‘Modifications to the List of Recognized Standards, Recognition List Number: 032’’ (Recognition List Number: 032), will assist manufacturers who elect to declare conformity with consensus standards to meet certain requirements for medical devices. DATES: Submit written or electronic comments concerning this document at any time. See section VII for the SUMMARY: PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 effective date of the recognition of standards announced in this document. ADDRESSES: Submit written requests for single copies of ‘‘Modifications to the List of Recognized Standards, Recognition List Number: 032’’ to the Division of Small Manufacturers, International and Consumer Assistance, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Silver Spring, MD 20993. Send two selfaddressed adhesive labels to assist that office in processing your requests, or fax your request to 301–847–8149. Submit written comments concerning this document, or recommendations for additional standards for recognition, to the contact person (see FOR FURTHER INFORMATION CONTACT). Submit electronic comments by email: standards@cdrh.fda.gov. This document may also be accessed on FDA’s Internet site at https://www.fda.gov/ MedicalDevices/ DeviceRegulationandGuidance/ Standards/ucm123792.htm. See section VI for electronic access to the searchable database for the current list of FDA recognized consensus standards, including Recognition List Number: 032 modifications and other standards related information. FOR FURTHER INFORMATION CONTACT: Scott A. Colburn, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 3632, Silver Spring, MD 20993, 301–796–6287. SUPPLEMENTARY INFORMATION: I. Background Section 204 of the Food and Drug Administration Modernization Act of 1997 (FDAMA) (Pub. L. 105–115) amended section 514 of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 360d). Amended section 514 allows FDA to recognize consensus standards developed by international and national organizations for use in satisfying portions of device premarket review submissions or other requirements. In a notice published in the Federal Register of February 25, 1998 (63 FR 9561), FDA announced the availability of a guidance entitled ‘‘Recognition and Use of Consensus Standards.’’ The notice described how FDA would implement its standard recognition program and provided the initial list of recognized standards. Modifications to the initial list of recognized standards, as published in the Federal Register, can be accessed at https://www.fda.gov/MedicalDevices/ E:\FR\FM\06AUN1.SGM 06AUN1 Federal Register / Vol. 78, No. 151 / Tuesday, August 6, 2013 / Notices DeviceRegulationandGuidance/ Standards/ucm123792.htm. These notices describe the addition, withdrawal, and revision of certain standards recognized by FDA. The Agency maintains ‘‘hypertext markup language (HTML)’’ and ‘‘portable document format (PDF)’’ versions of the list of ‘‘FDA Recognized Consensus Standards.’’ Both versions are publicly accessible at the Agency’s Internet site. See section VI for electronic access information. Interested persons should review the supplementary information sheet for the standard to understand fully the extent to which FDA recognizes the standard. II. Modifications to the List of Recognized Standards, Recognition List Number: 032 FDA is announcing the addition, withdrawal, correction, and revision of certain consensus standards the Agency will recognize for use in premarket submissions and other requirements for devices. FDA will incorporate these modifications in the list of FDA Recognized Consensus Standards in the Agency’s searchable database. FDA will 47713 use the term ‘‘Recognition List Number: 032’’ to identify these current modifications. In section III, FDA lists modifications the Agency is making that involve the initial addition of standards not previously recognized by FDA. III. Listing of New Entries In table 1, FDA provides the listing of new entries and consensus standards added as modifications to the list of recognized standards under Recognition List Number: 032. TABLE 1—NEW ENTRIES TO THE LIST OF RECOGNIZED STANDARDS Recognition No. Title of standard 1 Reference No. and date Software/Informatics 13–38 ............. 13–39 ............. 13–40 ............. 13–41 ............. 13–42 ............. 13–43 ............. 13–44 ............. 13–45 ............. 13–46 ............. 13–47 ............. 13–48 ............. 13–49 ............. 13–50 ............. 13–51 ............. 13–52 ............. 13–53 ............. 13–54 ............. 13–55 ............. tkelley on DSK3SPTVN1PROD with NOTICES 13–56 ............. 13–57 ............. 13–58 ............. 13–59 ............. 13–60 ............. VerDate Mar<15>2010 Application of risk management for IT networks incorporating medical devices— Part 1: Roles, responsibilities and activities. Application of risk management for IT networks incorporating medical devices— Part 1: Roles, responsibilities and activities. Application of risk management for IT networks incorporating medical devices— Part 2–1: Step-by-step risk management of medical IT networks—Practical applications and examples. Application of risk management for IT networks incorporating medical devices— Part 2–1: Step by step risk management of medical IT networks; Practical applications and examples. Application of risk management for IT networks incorporating medical devices— Part 2–2: Guidance for the disclosure and communication of medical device security needs, risks and controls. Application of risk management for IT networks incorporating medical devices— Part 2–2: Guidance for the disclosure and communication of medical device security needs, risks and controls. Application of risk management for IT networks incorporating medical devices— Part 2–3: Guidance for wireless networks. Application of risk management for IT networks incorporating medical devices— Part 2–3: Guidance for wireless networks. Medical Devices and Medical Systems—Essential safety requirements for equipment comprising the patient-centric integrated clinical environment (ICE)—Part 1: General requirements and conceptual model. Health informatics—Point-of-care medical device communication—Part 10101: Nomenclature. Health informatics—Point-of-care medical device communication—Part 10201: Domain information model. Health informatics—Point-of-care medical device communication—Part 20101: Application Profiles—Base Standard. Health informatics—Personal health device communication—Part 20601: Application profile—Optimized exchange protocol. Health informatics—Personal health device communication—Part 20601: Application profile—Optimized Exchange Protocol Amendment 1. Health informatics—Point-of-care medical device communication—Part 10408: Device specialization—Thermometer. Health informatics—Point-of-care medical device communication—Part 10415: Device specialization—Weighing scale. Health informatics—Personal health device communication—Part 10404: Device specialization—Pulse oximeter. Health informatics—Personal health device communication—Part 10421: Device specialization—Peak expiratory flow monitor (peak flow). Health informatics—Personal health device communication—Part 10406: Device specialization—Basic electrocardiograph (ECG) (1- to 3-lead ECG). Health informatics—Personal health device communication—Part 10407: Device specialization—Blood pressure monitor. Health informatics—Personal health device communication—Part 10417: Device specialization—Glucose meter. Systems and software engineering—Systems and software assurance—Part 4: Assurance in the life cycle. Industrial communication networks—Network and system security—Part 1–1: Terminology, concepts and models. 19:47 Aug 05, 2013 Jkt 229001 PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 IEC 80001–1 Edition 1.0 2010–10 ANSI/AAMI/IEC 80001–1:2010 IEC/TR 80001–2–1 Edition 1.0 2012–07 ANSI/AAMI/IEC TIR80001–2–1:2012 IEC/TR 80001–2–2 Edition 1.0 2012–07 ANSI/AAMI/IEC TIR80001–2–2:2012 IEC/TR 80001–2–3 Edition 1.0 2012–07 ANSI/AAMI/IEC TIR80001–2–3:2012 ASTM F2761–09 ISO/IEEE 11073–10101 First 2004–12–15 ISO/IEEE 11073–10201 First 2004–12–15 ISO/IEEE 11073–20101 First 2004–12–15 ISO/IEEE 11073–20601 First 2010–05–01 IEEE Std 11073–20601a-2010 edition ISO/IEEE 11073–10408 First 2010–05–01 ISO/IEEE 11073–10415 First 2010–05–01 ISO/IEEE 11073–10404 First 2010–05–01 IEEE Std 11073–10421–2010 edition edition edition edition edition edition IEEE Std 11073–10406–2011 ISO/IEEE 11073–10407 First edition 2010–05–01 ISO/IEEE 11073–10417 First edition 2010–05–01 ISO/IEC 15026–4 First edition 2012–10– 01 IEC/TS 62443–1–1 Edition 1.0 2009–07 E:\FR\FM\06AUN1.SGM 06AUN1 47714 Federal Register / Vol. 78, No. 151 / Tuesday, August 6, 2013 / Notices TABLE 1—NEW ENTRIES TO THE LIST OF RECOGNIZED STANDARDS—Continued Recognition No. Title of standard 1 13–61 ............. Industrial communication networks—Network and system security—Part 2–1: Establishing an industrial automation and control system security program. Industrial communication networks—Network and system security—Part 3–1: Security technologies for industrial automation and control systems. 13–62 ............. 1 All IEC 62443–2–1 Edition 1.0 2010–11 IEC/TR 62443–3–1 Edition 1.0 2009–07 standard titles in this table conform to the style requirements of the respective organizations. IV. List of Recognized Standards FDA maintains the Agency’s current list of FDA recognized consensus standards in a searchable database that may be accessed directly at FDA’s Internet site at https:// www.accessdata.fda.gov/scripts/cdrh/ cfdocs/cfStandards/search.cfm. FDA will incorporate the modifications and revisions described into the database and, upon publication in the Federal Register, this recognition of consensus standards will be effective. FDA will announce additional modifications and revisions to the list of recognized consensus standards, as needed, in the Federal Register once a year, or more often, if necessary. Beginning with Recognition List Number: 033, FDA will no longer be announcing minor revisions to the list of recognized consensus standards such as technical contact person, relevant guidance, processes affected, CFR citations, and product codes. tkelley on DSK3SPTVN1PROD with NOTICES Reference No. and date V. Recommendation of Standards for Recognition by FDA Any person may recommend consensus standards as candidates for recognition under section 514 of the FD&C Act by submitting such recommendations, with reasons for the recommendation, to the contact person (see FOR FURTHER INFORMATION CONTACT). To be properly considered, such recommendations should contain, at a minimum, the following information: (1) Title of the standard; (2) any reference number and date; (3) name and address of the national or international standards development organization; (4) a proposed list of devices for which a declaration of conformity to this standard should routinely apply; and (5) a brief identification of the testing or performance or other characteristics of the device(s) that would be addressed by a declaration of conformity. VI. Electronic Access You may obtain a copy of ‘‘Guidance on the Recognition and Use of Consensus Standards’’ by using the Internet. The Center for Devices and Radiological Health (CDRH) maintains a VerDate Mar<15>2010 19:47 Aug 05, 2013 Jkt 229001 site on the Internet for easy access to information including text, graphics, and files that you may download to a personal computer with access to the Internet. Updated on a regular basis, the CDRH home page includes the guidance as well as the current list of recognized standards and other standards-related documents. After publication in the Federal Register, this notice announcing ‘‘Modification to the List of Recognized Standards, Recognition List Number: 032’’ will be available on the CDRH home page. You may access the CDRH home page at https://www.fda.gov/ MedicalDevices. You may access ‘‘Guidance on the Recognition and Use of Consensus Standards,’’ and the searchable database for ‘‘FDA Recognized Consensus Standards’’ at https://www.fda.gov/ MedicalDevices/ DeviceRegulationandGuidance/ Standards. This Federal Register document on modifications in FDA’s recognition of consensus standards is available at https://www.fda.gov/MedicalDevices/ DeviceRegulationandGuidance/ Standards/ucm123792.htm. VII. Submission of Comments and Effective Date Interested persons may submit to the contact person (see FOR FURTHER INFORMATION CONTACT) either electronic or written comments regarding this document. It is only necessary to send one set of comments. Comments are to be identified with the docket number found in brackets in the heading of this document. FDA will consider any comments received in determining whether to amend the current listing of modifications to the list of recognized standards, Recognition List Number: 032. These modifications to the list of recognized standards are effective upon publication of this notice in the Federal Register. Dated: July 31, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013–19020 Filed 8–5–13; 8:45 am] BILLING CODE 4160–01–P PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Advisory Council on Blood Stem Cell Transplantation; Notice of Meeting In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), notice is hereby given of the following meeting: Name: Advisory Council on Blood Stem Cell Transplantation. Date and Time: September 13, 2013, 10:00 a.m. to 4:00 p.m. (Eastern Standard Time). Place: The meeting will be via audio conference call and Adobe Connect Pro. Status: The meeting will be open to the public. Purpose: Pursuant to Public Law 109– 129, 42 U.S.C. 274k (section 379 of the Public Health Service Act, as amended), the Advisory Council on Blood Stem Cell Transplantation (ACBSCT) advises the Secretary of the Department of Health and Human Services and the Administrator, Health Resources and Services Administration on matters related to the activities of the C.W. Bill Young Cell Transplantation Program (Program) and the National Cord Blood Inventory Program. Agenda: The Council will hear reports from ACBSCT Work Groups including: Cord Blood Thawing and Washing; Access to Transplantation; and Advancing Hematopoietic Stem Cell Transplantation for Hemoglobinopathies. The Council also will hear presentations and discussions on topics including: Accreditation; Adverse Event Reporting; and Unmet Need. Agenda items are subject to change as priorities indicate. After Council discussions, members of the public will have an opportunity to provide comments. Because of the Council’s full agenda and the time frame in which to cover the agenda topics, public comment will be limited. All public comments will be included in the record of the ACBSCT meeting. Meeting summary notes will be posted on the HRSA’s Program Web site at E:\FR\FM\06AUN1.SGM 06AUN1

Agencies

[Federal Register Volume 78, Number 151 (Tuesday, August 6, 2013)]
[Notices]
[Pages 47712-47714]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-19020]

-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2004-N-0451] (formerly 2004N-0226)

Food and Drug Administration Modernization Act of 1997:
Modifications to the List of Recognized Standards, Recognition List
Number: 032

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is announcing a
publication containing modifications the Agency is making to the list
of standards FDA recognizes for use in premarket reviews (FDA
recognized consensus standards). Specifically, this publication
announces the addition of a list of recognized standards that are
relevant to interoperability of medical devices. This publication,
entitled ``Modifications to the List of Recognized Standards,
Recognition List Number: 032'' (Recognition List Number: 032), will
assist manufacturers who elect to declare conformity with consensus
standards to meet certain requirements for medical devices.

DATES: Submit written or electronic comments concerning this document
at any time. See section VII for the effective date of the recognition
of standards announced in this document.

ADDRESSES: Submit written requests for single copies of ``Modifications
to the List of Recognized Standards, Recognition List Number: 032'' to
the Division of Small Manufacturers, International and Consumer
Assistance, Center for Devices and Radiological Health, Food and Drug
Administration, 10903 New Hampshire Ave., Bldg. 66, Silver Spring, MD
20993. Send two self-addressed adhesive labels to assist that office in
processing your requests, or fax your request to 301-847-8149. Submit
written comments concerning this document, or recommendations for
additional standards for recognition, to the contact person (see FOR
FURTHER INFORMATION CONTACT). Submit electronic comments by email:
standards@cdrh.fda.gov. This document may also be accessed on FDA's
Internet site at https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Standards/ucm123792.htm. See section VI for
electronic access to the searchable database for the current list of
FDA recognized consensus standards, including Recognition List Number:
032 modifications and other standards related information.

FOR FURTHER INFORMATION CONTACT: Scott A. Colburn, Center for Devices
and Radiological Health, Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 66, Rm. 3632, Silver Spring, MD 20993, 301-796-
6287.

SUPPLEMENTARY INFORMATION:

I. Background

Section 204 of the Food and Drug Administration Modernization Act
of 1997 (FDAMA) (Pub. L. 105-115) amended section 514 of the Federal
Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 360d). Amended
section 514 allows FDA to recognize consensus standards developed by
international and national organizations for use in satisfying portions
of device premarket review submissions or other requirements.
In a notice published in the Federal Register of February 25, 1998
(63 FR 9561), FDA announced the availability of a guidance entitled
``Recognition and Use of Consensus Standards.'' The notice described
how FDA would implement its standard recognition program and provided
the initial list of recognized standards.
Modifications to the initial list of recognized standards, as
published in the Federal Register, can be accessed at https://
www.fda.gov/MedicalDevices/

[[Page 47713]]

DeviceRegulationandGuidance/Standards/ucm123792.htm.
These notices describe the addition, withdrawal, and revision of
certain standards recognized by FDA. The Agency maintains ``hypertext
markup language (HTML)'' and ``portable document format (PDF)''
versions of the list of ``FDA Recognized Consensus Standards.'' Both
versions are publicly accessible at the Agency's Internet site. See
section VI for electronic access information. Interested persons should
review the supplementary information sheet for the standard to
understand fully the extent to which FDA recognizes the standard.

II. Modifications to the List of Recognized Standards, Recognition List
Number: 032

FDA is announcing the addition, withdrawal, correction, and
revision of certain consensus standards the Agency will recognize for
use in premarket submissions and other requirements for devices. FDA
will incorporate these modifications in the list of FDA Recognized
Consensus Standards in the Agency's searchable database. FDA will use
the term ``Recognition List Number: 032'' to identify these current
modifications.
In section III, FDA lists modifications the Agency is making that
involve the initial addition of standards not previously recognized by
FDA.

III. Listing of New Entries

In table 1, FDA provides the listing of new entries and consensus
standards added as modifications to the list of recognized standards
under Recognition List Number: 032.

Table 1--New Entries to the List of Recognized Standards
----------------------------------------------------------------------------------------------------------------
Recognition No. Title of standard \1\ Reference No. and date
----------------------------------------------------------------------------------------------------------------
Software/Informatics
----------------------------------------------------------------------------------------------------------------
13-38...................... Application of risk management for IT networks IEC 80001-1 Edition 1.0 2010-
incorporating medical devices--Part 1: Roles, 10
responsibilities and activities.
13-39...................... Application of risk management for IT networks ANSI/AAMI/IEC 80001-1:2010
incorporating medical devices--Part 1: Roles,
responsibilities and activities.
13-40...................... Application of risk management for IT networks IEC/TR 80001-2-1 Edition 1.0
incorporating medical devices--Part 2-1: Step-by- 2012-07
step risk management of medical IT networks--
Practical applications and examples.
13-41...................... Application of risk management for IT networks ANSI/AAMI/IEC TIR80001-2-
incorporating medical devices--Part 2-1: Step by 1:2012
step risk management of medical IT networks;
Practical applications and examples.
13-42...................... Application of risk management for IT networks IEC/TR 80001-2-2 Edition 1.0
incorporating medical devices--Part 2-2: Guidance 2012-07
for the disclosure and communication of medical
device security needs, risks and controls.
13-43...................... Application of risk management for IT networks ANSI/AAMI/IEC TIR80001-2-
incorporating medical devices--Part 2-2: Guidance 2:2012
for the disclosure and communication of medical
device security needs, risks and controls.
13-44...................... Application of risk management for IT networks IEC/TR 80001-2-3 Edition 1.0
incorporating medical devices--Part 2-3: Guidance 2012-07
for wireless networks.
13-45...................... Application of risk management for IT networks ANSI/AAMI/IEC TIR80001-2-
incorporating medical devices--Part 2-3: Guidance 3:2012
for wireless networks.
13-46...................... Medical Devices and Medical Systems--Essential ASTM F2761-09
safety requirements for equipment comprising the
patient-centric integrated clinical environment
(ICE)--Part 1: General requirements and conceptual
model.
13-47...................... Health informatics--Point-of-care medical device ISO/IEEE 11073-10101 First
communication--Part 10101: Nomenclature. edition 2004-12-15
13-48...................... Health informatics--Point-of-care medical device ISO/IEEE 11073-10201 First
communication--Part 10201: Domain information edition 2004-12-15
model.
13-49...................... Health informatics--Point-of-care medical device ISO/IEEE 11073-20101 First
communication--Part 20101: Application Profiles-- edition 2004-12-15
Base Standard.
13-50...................... Health informatics--Personal health device ISO/IEEE 11073-20601 First
communication--Part 20601: Application profile-- edition 2010-05-01
Optimized exchange protocol.
13-51...................... Health informatics--Personal health device IEEE Std 11073-20601a-2010
communication--Part 20601: Application profile--
Optimized Exchange Protocol Amendment 1.
13-52...................... Health informatics--Point-of-care medical device ISO/IEEE 11073-10408 First
communication--Part 10408: Device specialization-- edition 2010-05-01
Thermometer.
13-53...................... Health informatics--Point-of-care medical device ISO/IEEE 11073-10415 First
communication--Part 10415: Device specialization-- edition 2010-05-01
Weighing scale.
13-54...................... Health informatics--Personal health device ISO/IEEE 11073-10404 First
communication--Part 10404: Device specialization-- edition 2010-05-01
Pulse oximeter.
13-55...................... Health informatics--Personal health device IEEE Std 11073-10421-2010
communication--Part 10421: Device specialization--
Peak expiratory flow monitor (peak flow).
13-56...................... Health informatics--Personal health device IEEE Std 11073-10406-2011
communication--Part 10406: Device specialization--
Basic electrocardiograph (ECG) (1- to 3-lead ECG).
13-57...................... Health informatics--Personal health device ISO/IEEE 11073-10407 First
communication--Part 10407: Device specialization-- edition 2010-05-01
Blood pressure monitor.
13-58...................... Health informatics--Personal health device ISO/IEEE 11073-10417 First
communication--Part 10417: Device specialization-- edition 2010-05-01
Glucose meter.
13-59...................... Systems and software engineering--Systems and ISO/IEC 15026-4 First edition
software assurance--Part 4: Assurance in the life 2012-10-01
cycle.
13-60...................... Industrial communication networks--Network and IEC/TS 62443-1-1 Edition 1.0
system security--Part 1-1: Terminology, concepts 2009-07
and models.

[[Page 47714]]

13-61...................... Industrial communication networks--Network and IEC 62443-2-1 Edition 1.0 2010-
system security--Part 2-1: Establishing an 11
industrial automation and control system security
program.
13-62...................... Industrial communication networks--Network and IEC/TR 62443-3-1 Edition 1.0
system security--Part 3-1: Security technologies 2009-07
for industrial automation and control systems.
----------------------------------------------------------------------------------------------------------------
\1\ All standard titles in this table conform to the style requirements of the respective organizations.

IV. List of Recognized Standards

FDA maintains the Agency's current list of FDA recognized consensus
standards in a searchable database that may be accessed directly at
FDA's Internet site at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfStandards/search.cfm. FDA will incorporate the modifications
and revisions described into the database and, upon publication in the
Federal Register, this recognition of consensus standards will be
effective. FDA will announce additional modifications and revisions to
the list of recognized consensus standards, as needed, in the Federal
Register once a year, or more often, if necessary. Beginning with
Recognition List Number: 033, FDA will no longer be announcing minor
revisions to the list of recognized consensus standards such as
technical contact person, relevant guidance, processes affected, CFR
citations, and product codes.

V. Recommendation of Standards for Recognition by FDA

Any person may recommend consensus standards as candidates for
recognition under section 514 of the FD&C Act by submitting such
recommendations, with reasons for the recommendation, to the contact
person (see FOR FURTHER INFORMATION CONTACT). To be properly
considered, such recommendations should contain, at a minimum, the
following information: (1) Title of the standard; (2) any reference
number and date; (3) name and address of the national or international
standards development organization; (4) a proposed list of devices for
which a declaration of conformity to this standard should routinely
apply; and (5) a brief identification of the testing or performance or
other characteristics of the device(s) that would be addressed by a
declaration of conformity.

VI. Electronic Access

You may obtain a copy of ``Guidance on the Recognition and Use of
Consensus Standards'' by using the Internet. The Center for Devices and
Radiological Health (CDRH) maintains a site on the Internet for easy
access to information including text, graphics, and files that you may
download to a personal computer with access to the Internet. Updated on
a regular basis, the CDRH home page includes the guidance as well as
the current list of recognized standards and other standards-related
documents. After publication in the Federal Register, this notice
announcing ``Modification to the List of Recognized Standards,
Recognition List Number: 032'' will be available on the CDRH home page.
You may access the CDRH home page at https://www.fda.gov/MedicalDevices.
You may access ``Guidance on the Recognition and Use of Consensus
Standards,'' and the searchable database for ``FDA Recognized Consensus
Standards'' at https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Standards.
This Federal Register document on modifications in FDA's
recognition of consensus standards is available at https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Standards/ucm123792.htm.

VII. Submission of Comments and Effective Date

Interested persons may submit to the contact person (see FOR
FURTHER INFORMATION CONTACT) either electronic or written comments
regarding this document. It is only necessary to send one set of
comments. Comments are to be identified with the docket number found in
brackets in the heading of this document. FDA will consider any
comments received in determining whether to amend the current listing
of modifications to the list of recognized standards, Recognition List
Number: 032. These modifications to the list of recognized standards
are effective upon publication of this notice in the Federal Register.

Dated: July 31, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-19020 Filed 8-5-13; 8:45 am]
BILLING CODE 4160-01-P

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