Adoption of Updated EDGAR Filer Manual, 13216-13218 [2014-05057]
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13216
Federal Register / Vol. 79, No. 46 / Monday, March 10, 2014 / Rules and Regulations
Based upon the number of laboratories
in the United States that have applied
for CPSC acceptance of the accreditation
to test for conformance to other juvenile
product standards, we expect that only
a few laboratories will seek CPSC
acceptance of their accreditation to test
for conformance with the standard for
carriages and strollers. Most of these
laboratories already will have been
accredited to test for conformance to
other juvenile product standards, and
the only cost to them would be the cost
of adding the standard for carriages and
strollers to their scope of accreditation.
As a consequence, the Commission
certifies that the NOR for the standard
for carriages and strollers will not have
a significant impact on a substantial
number of small entities.
List of Subjects
16 CFR Part 1112
Administrative practice and
procedure, Audit, Consumer protection,
Reporting and recordkeeping
requirements, Third party conformity
assessment body.
16 CFR Part 1227
Consumer protection, Imports,
Incorporation by reference, Infants and
children, Labeling, Law enforcement,
and Toys.
For the reasons discussed in the
preamble, the Commission amends Title
16 of the Code of Federal Regulations as
follows:
PART 1112—REQUIREMENTS
PERTAINING TO THIRD PARTY
CONFORMITY ASSESSMENT BODIES
1. The authority citation for part 1112
continues to read as follows:
■
Authority: 15 U.S.C. 2063; Pub. L. 110–
314, section 3, 122 Stat. 3016, 3017 (2008).
2. Amend § 1112.15 by adding
paragraph (b)(36) to read as follows:
■
§ 1112.15 When can a third party
conformity assessment body apply for
CPSC acceptance for a particular CPSC rule
and/or test method?
*
*
*
*
(b)(36) 16 CFR part 1227, Safety
Standard for Carriages and Strollers.
*
*
*
*
*
■ 3. Add part 1227 to read as follows:
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*
PART 1227—SAFETY STANDARD FOR
CARRIAGES AND STROLLERS
Sec.
1227.1 Scope.
1227.2 Requirements for carriages and
strollers.
Authority: The Consumer Product Safety
Improvement Act of 2008, Pub. L. 110–314,
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§ 104, 122 Stat. 3016 (August 14, 2008); Pub.
L. 112–28, 125 Stat. 273 (August 12, 2011).
§ 1227.1
Scope.
This part establishes a consumer
product safety standard for carriages
and strollers.
§ 1227.2 Requirements for carriages and
strollers.
(a) Except as provided in paragraph
(b) of this section, each carriage and
stroller must comply with all applicable
provisions of ASTM F833–13b,
Standard Consumer Safety Performance
Specification for Carriages and Strollers,
approved on November 1, 2013. The
Director of the Federal Register
approves this incorporation by reference
in accordance with 5 U.S.C. 552(a) and
1 CFR part 51. You may obtain a copy
from ASTM International, 100 Bar
Harbor Drive, P.O. Box 0700, West
Conshohocken, PA 19428; https://
www.astm.org/cpsc.htm. You may
inspect a copy at the Office of the
Secretary, U.S. Consumer Product
Safety Commission, Room 820, 4330
East West Highway, Bethesda, MD
20814, telephone 301–504–7923, or at
the National Archives and Records
Administration (NARA). For
information on the availability of this
material at NARA, call 202–741–6030,
or go to: https://www.archives.gov/
federal_register/code_of_federal
regulations/ibr_locations.html.
(b) Comply with ASTM F833–13b
standard with the following changes:
(1) Instead of complying with section
7.12.1 of ASTM F833–13b, comply with
the following:
(i) 7.12.1 Secure the front wheels of
the unit in their normal standing
position so that the unit cannot move
forward. Attach the tray(s) or grab bar(s)
in the position that creates the bounded
opening(s). Position any adjustable
features (that is, grab bar, calf supports,
foot rests, etc.) that may affect the
bounded opening(s) to create an
opening(s) size that is most likely to
cause failure.
(ii) [Reserved]
(2) Instead of complying with section
7.12.3 of ASTM F833–13b, comply with
the following:
(i) 7.12.3 If necessary, reattach/
reposition tray(s) grab bar(s), then
perform the torso probe test per 7.12.4.
Position any adjustable features (that is,
grab bar, calf supports, foot rests, etc.)
that may affect the bounded opening(s),
to create the opening(s) size that is most
likely to cause failure.
(ii) [Reserved]
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Dated: March 5, 2014.
Todd A. Stevenson,
Secretary, Consumer Product Safety
Commission.
[FR Doc. 2014–05065 Filed 3–7–14; 8:45 am]
BILLING CODE 6355–01–P
SECURITIES AND EXCHANGE
COMMISSION
17 CFR Part 232
[Release Nos. 33–9554; 34–71643; 39–2496;
IC–30972]
Adoption of Updated EDGAR Filer
Manual
Securities and Exchange
Commission.
ACTION: Final rule.
AGENCY:
The Securities and Exchange
Commission (the Commission) is
adopting revisions to the Electronic Data
Gathering, Analysis, and Retrieval
System (EDGAR) Filer Manual and
related rules to reflect updates to the
EDGAR system. The revisions are being
made primarily to introduce new
submission form types MA, MA–A, MA/
A, MA–I, MA–I/A, and MA–W to
support Registration of Municipal
Advisors; updates to submission form
types 8–K, 8–K/A, 10–K, 10–K/A, 10–
KT, 10–KT/A, 10–D, 10–D/A, POS AM,
424B1, 424B2, 424B3, 424B4, 424B5,
424B7, and 424B8; and minor updates
to Form 13F validations. The EDGAR
system is scheduled to be upgraded to
support this functionality on March 3,
2014.
DATES: Effective Date: March 10, 2014.
The incorporation by reference of the
EDGAR Filer Manual is approved by the
Director of the Federal Register as of
March 10, 2014.
FOR FURTHER INFORMATION CONTACT: In
the Office of Municipal Securities, for
questions concerning Registration of
Municipal Advisors contact Jessica
Kane at (202) 551–3235; in the Division
of Investment Management, for
questions concerning Form 13F contact
Heather Fernandez at (202) 551–6715;
and in the Office of Information
Technology, contact Vanessa Anderson
at (202) 551–8800.
SUPPLEMENTARY INFORMATION: We are
adopting an updated EDGAR Filer
Manual, Volume I and Volume II. The
Filer Manual describes the technical
formatting requirements for the
preparation and submission of
electronic filings through the EDGAR
system.1 It also describes the
SUMMARY:
1 We originally adopted the Filer Manual on April
1, 1993, with an effective date of April 26, 1993.
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Federal Register / Vol. 79, No. 46 / Monday, March 10, 2014 / Rules and Regulations
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requirements for filing using
EDGARLink Online and the Online
Forms/XML Web site.
The revisions to the Filer Manual
reflect changes within Volume I entitled
EDGAR Filer Manual, Volume I:
‘‘General Information,’’ Version 16
(March 2014) and Volume II entitled
EDGAR Filer Manual, Volume II:
‘‘EDGAR Filing,’’ Version 26 (March
2014). The updated manual will be
incorporated by reference into the Code
of Federal Regulations.
The Filer Manual contains all the
technical specifications for filers to
submit filings using the EDGAR system.
Filers must comply with the applicable
provisions of the Filer Manual in order
to assure the timely acceptance and
processing of filings made in electronic
format.2 Filers may consult the Filer
Manual in conjunction with our rules
governing mandated electronic filing
when preparing documents for
electronic submission.3
The EDGAR system will be upgraded
to Release 14.0 on March 3, 2014 and
will introduce the following changes:
EDGAR will be updated to add new
submission form types MA, MA–A, MA/
A, MA–I, MA–I/A, and MA–W on the
EDGAR Filing Web site. These
submission form types can be accessed
by selecting the ‘File Municipal Advisor
Forms’ link available on the EDGAR
Filing Web site. Instructions to file the
Municipal Advisor Forms are included
in two new sections of Chapter 9
(Preparing and Transmitting Online
Submissions) of the ‘‘EDGAR Filer
Manual, Volume II: EDGAR Filing’’ to
guide filers through the filing process.
See Release No. 34–70462 4 for the
compliance dates.
Submission form types 8–K, 8–K/A,
10–K, 10–K/A, 10–KT, 10–KT/A, 10–D,
10–D/A, POS AM, 424B1, 424B2,
424B3, 424B4, 424B5, 424B7, and 424B8
will be updated to collect Depositor
CIK, Sponsor CIK, ABS Asset Class, and
ABS Sub Asset Class information for
filings where the primary registrant CIK
is designated as an Asset-Backed
Securities issuing entity (i.e., entities
assigned the Standard Industrial
Classification Code 6189).
Submission form types 13F–HR/A
will be updated to allow a future date
for the ‘‘Date denied or on which
confidential treatment expired’’ field.
For EDGARLink Online application,
recommended version for Firefox
browser is being changed from 3.5 to
17.0 or higher. For all EDGAR Web sites,
Microsoft Internet Explorer 7.0 or later
is the recommended browser.
Additionally, minor documentation
only corrections were made to the
Chapter 6, Interactive Data, sections
6.5.20 and 6.6.29.
Along with the adoption of the Filer
Manual, we are amending Rule 301 of
Regulation S–T to provide for the
incorporation by reference into the Code
of Federal Regulations of today’s
revisions. This incorporation by
reference was approved by the Director
of the Federal Register in accordance
with 5 U.S.C. 552(a) and 1 CFR Part 51.
You may obtain paper copies of the
updated Filer Manual at the following
address: Public Reference Room, U.S.
Securities and Exchange Commission,
100 F Street NE., Room 1543,
Washington, DC 20549, on official
business days between the hours of
10:00 a.m. and 3:00 p.m. We will post
electronic format copies on the
Commission’s Web site; the address for
the Filer Manual is https://www.sec.gov/
info/edgar.shtml.
Since the Filer Manual and the
corresponding rule changes relate solely
to agency procedures or practice,
publication for notice and comment is
not required under the Administrative
Procedure Act (APA).5 It follows that
the requirements of the Regulatory
Flexibility Act 6 do not apply.
The effective date for the updated
Filer Manual and the rule amendments
is March 10, 2014. In accordance with
the APA,7 we find that there is good
cause to establish an effective date less
than 30 days after publication of these
rules. The EDGAR system upgrade to
Release 14.0 is scheduled to become
available on March 3, 2014. The
Commission believes that establishing
an effective date less than 30 days after
publication of these rules is necessary to
coordinate the effectiveness of the
updated Filer Manual with the system
upgrade.
Release No. 33–6986 (April 1, 1993) [58 FR 18638].
We implemented the most recent update to the Filer
Manual on September 25, 2013. See Release No. 33–
9457 (October 2, 2013) [78 FR 60684].
2 See Rule 301 of Regulation S–T (17 CFR
232.301).
3 See Release No. 33–9457 in which we
implemented EDGAR Release 13.3. For additional
history of Filer Manual rules, please see the cites
therein.
4 See Release No. 34–70462 (September 20, 2013)
[78 FR 67467 (November 12, 2013)].
We are adopting the amendments to
Regulation S–T under Sections 6, 7, 8,
10, and 19(a) of the Securities Act of
1933,8 Sections 3, 12, 13, 14, 15, 23, and
35A of the Securities Exchange Act of
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Statutory Basis
U.S.C. 553(b).
U.S.C. 601–612.
7 5 U.S.C. 553(d)(3).
8 15 U.S.C. 77f, 77g, 77h, 77j, and 77s(a).
13217
1934,9 Section 319 of the Trust
Indenture Act of 1939,10 and Sections 8,
30, 31, and 38 of the Investment
Company Act of 1940.11
List of Subjects in 17 CFR Part 232
Incorporation by reference, Reporting
and recordkeeping requirements,
Securities.
Text of the Amendment
In accordance with the foregoing,
Title 17, Chapter II of the Code of
Federal Regulations is amended as
follows:
PART 232—REGULATION S–T—
GENERAL RULES AND REGULATIONS
FOR ELECTRONIC FILINGS
1. The authority citation for Part 232
continues to read in part as follows:
■
Authority: 15 U.S.C. 77f, 77g, 77h, 77j,
77s(a), 77z–3, 77sss(a), 78c(b), 78l, 78m, 78n,
78o(d), 78w(a), 78ll, 80a–6(c), 80a–8, 80a–29,
80a–30, 80a–37, and 7201 et seq.; and 18
U.S.C. 1350.
*
*
*
*
*
2. Section 232.301 is revised to read
as follows:
■
§ 232.301
EDGAR Filer Manual.
Filers must prepare electronic filings
in the manner prescribed by the EDGAR
Filer Manual, promulgated by the
Commission, which sets out the
technical formatting requirements for
electronic submissions. The
requirements for becoming an EDGAR
Filer and updating company data are set
forth in the updated EDGAR Filer
Manual, Volume I: ‘‘General
Information,’’ Version 16 (March 2014).
The requirements for filing on EDGAR
are set forth in the updated EDGAR Filer
Manual, Volume II: ‘‘EDGAR Filing,’’
Version 26 (March 2014). Additional
provisions applicable to Form N–SAR
filers are set forth in the EDGAR Filer
Manual, Volume III: ‘‘N–SAR
Supplement,’’ Version 2 (August 2011).
All of these provisions have been
incorporated by reference into the Code
of Federal Regulations, which action
was approved by the Director of the
Federal Register in accordance with 5
U.S.C. 552(a) and 1 CFR Part 51. You
must comply with these requirements in
order for documents to be timely
received and accepted. You can obtain
paper copies of the EDGAR Filer
Manual from the following address:
Public Reference Room, U.S. Securities
and Exchange Commission, 100 F Street
NE., Room 1543, Washington, DC
55
65
PO 00000
Frm 00029
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9 15
U.S.C. 78c, 78l, 78m, 78n, 78o, 78w, and 78ll.
U.S.C. 77sss.
11 15 U.S.C. 80a–8, 80a–29, 80a–30, and 80a–37.
10 15
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Federal Register / Vol. 79, No. 46 / Monday, March 10, 2014 / Rules and Regulations
20549, on official business days
between the hours of 10:00 a.m. and
3:00 p.m. Electronic copies are available
on the Commission’s Web site. The
address for the Filer Manual is https://
www.sec.gov/info/edgar.shtml. You can
also inspect the document at the
National Archives and Records
Administration (NARA). For
information on the availability of this
material at NARA, call 202–741–6030,
or go to: https://www.archives.gov/
federal_register/code_of_federal_
regulations/ibr_locations.html.
Dated: March 4, 2014.
By the Commission.
Elizabeth M. Murphy,
Secretary.
[FR Doc. 2014–05057 Filed 3–7–14; 8:45 am]
BILLING CODE 8011–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 878
[Docket No. FDA–2014–N–0107]
Medical Devices; General and Plastic
Surgery Devices; Classification of the
Absorbable Lung Biopsy Plug
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Final order.
The Food and Drug
Administration (FDA) is classifying the
absorbable lung biopsy plug into class II
(special controls). The special controls
that will apply to the device are
identified in this order, and will be part
of the codified language for the
absorbable lung biopsy plug’s
classification. The Agency is classifying
the device into class II (special controls)
in order to provide a reasonable
assurance of safety and effectiveness of
the device.
DATES: This order is effective April 9,
2014. The classification was effective on
December 19, 2012.
FOR FURTHER INFORMATION CONTACT: Neel
Patel, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. 2532, Silver Spring,
MD 20993–0002, 301–796–6274.
SUPPLEMENTARY INFORMATION:
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SUMMARY:
I. Background
In accordance with section 513(f)(1) of
the Federal Food, Drug, and Cosmetic
Act (the FD&C Act) (21 U.S.C.
360c(f)(1)), devices that were not in
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commercial distribution before May 28,
1976 (the date of enactment of the
Medical Device Amendments of 1976),
generally referred to as postamendments
devices, are classified automatically by
statute into class III without any FDA
rulemaking process. These devices
remain in class III and require
premarket approval, unless and until
the device is classified or reclassified
into class I or II, or FDA issues an order
finding the device to be substantially
equivalent, in accordance with section
513(i), to a predicate device that does
not require premarket approval. The
Agency determines whether new
devices are substantially equivalent to
predicate devices by means of
premarket notification procedures in
section 510(k) of the FD&C Act (21
U.S.C. 360(k)) and part 807 (21 CFR part
807) of the regulations.
Section 513(f)(2) of the FD&C Act, as
amended by section 607 of the Food and
Drug Administration Safety and
Innovation Act (Pub. L. 112–144, July 9,
2012, 126 Stat. 1054), provides two
procedures by which a person may
request FDA to classify a device under
the criteria set forth in section 513(a)(1).
Under the first procedure, the person
submits a premarket notification under
section 510(k) for a device that has not
previously been classified and, within
30 days of receiving an order classifying
the device into class III under section
513(f)(1), the person requests a
classification under section 513(f)(2).
Under the second procedure, rather than
first submitting a premarket notification
under section 510(k) and then a request
for classification under the first
procedure, the person determines that
there is no legally marketed device upon
which to base a determination of
substantial equivalence and requests a
classification under section 513(f)(2). If
the person submits a request to classify
the device under this second procedure,
FDA may decline to undertake the
classification request if FDA identifies a
legally marketed device that could
provide a reasonable basis for review of
substantial equivalence with the device
or if FDA determines that the device
submitted is not of ‘‘low-moderate risk’’
or that general controls would be
inadequate to control the risks and
special controls to mitigate the risks
cannot be developed.
In response to a request to classify a
device under either procedure provided
by section 513(f)(2) of the FD&C Act,
FDA will classify the device by written
order within 120 days. This
classification will be the initial
classification of the device.
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In accordance with section 513(f)(1) of
the FD&C Act, FDA issued an order on
March 19, 2009, classifying the Bio-Seal
Lung Biopsy Tract Plug System into
class III, because it was not substantially
equivalent to a device that was
introduced or delivered for introduction
into interstate commerce for commercial
distribution before May 28, 1976, or a
device which was subsequently
reclassified into class I or class II. On
April 16, 2009, Angiotech submitted a
request for classification of the Bio-Seal
Lung Biopsy Tract Plug System under
section 513(f)(2) of the FD&C Act. The
manufacturer recommended that the
device be classified into class II (Ref. 1).
In accordance with section 513(f)(2) of
the FD&C Act, FDA reviewed the
request in order to classify the device
under the criteria for classification set
forth in section 513(a)(1) of the FD&C
Act. FDA classifies devices into class II
if general controls by themselves are
insufficient to provide reasonable
assurance of safety and effectiveness but
there is sufficient information to
establish special controls to provide
reasonable assurance of the safety and
effectiveness of the device for its
intended use. After review of the
information submitted in the request,
FDA determined that the device can be
classified into class II with the
establishment of special controls. FDA
believes these special controls will
provide reasonable assurance of the
safety and effectiveness of the device.
Therefore, on December 19, 2012,
FDA issued an order to the requester
classifying the device into class II. FDA
is codifying the classification of the
device by adding 21 CFR 878.4755.
Following the effective date of this
final classification order, any firm
submitting a premarket notification
(510(k)) for an absorbable lung biopsy
plug will need to comply with the
special controls named in this final
order.
The device is assigned the generic
name Absorbable Lung Biopsy Plug, and
it is identified as a preformed
(polymerized) absorbable lung biopsy
plug intended to provide accuracy in
marking a biopsy location for
visualization during surgical resection
and closure of pleural punctures
associated with percutaneous,
transthoracic needle lung biopsies.
Upon deployment into the biopsy tract,
the plug expands to fill the biopsy void
and remains in place until resorbed.
FDA has identified the following risks
to health associated specifically with
this type of device, as well as the
mitigation measures.
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Agencies
[Federal Register Volume 79, Number 46 (Monday, March 10, 2014)]
[Rules and Regulations]
[Pages 13216-13218]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-05057]
=======================================================================
-----------------------------------------------------------------------
SECURITIES AND EXCHANGE COMMISSION
17 CFR Part 232
[Release Nos. 33-9554; 34-71643; 39-2496; IC-30972]
Adoption of Updated EDGAR Filer Manual
AGENCY: Securities and Exchange Commission.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The Securities and Exchange Commission (the Commission) is
adopting revisions to the Electronic Data Gathering, Analysis, and
Retrieval System (EDGAR) Filer Manual and related rules to reflect
updates to the EDGAR system. The revisions are being made primarily to
introduce new submission form types MA, MA-A, MA/A, MA-I, MA-I/A, and
MA-W to support Registration of Municipal Advisors; updates to
submission form types 8-K, 8-K/A, 10-K, 10-K/A, 10-KT, 10-KT/A, 10-D,
10-D/A, POS AM, 424B1, 424B2, 424B3, 424B4, 424B5, 424B7, and 424B8;
and minor updates to Form 13F validations. The EDGAR system is
scheduled to be upgraded to support this functionality on March 3,
2014.
DATES: Effective Date: March 10, 2014. The incorporation by reference
of the EDGAR Filer Manual is approved by the Director of the Federal
Register as of March 10, 2014.
FOR FURTHER INFORMATION CONTACT: In the Office of Municipal Securities,
for questions concerning Registration of Municipal Advisors contact
Jessica Kane at (202) 551-3235; in the Division of Investment
Management, for questions concerning Form 13F contact Heather Fernandez
at (202) 551-6715; and in the Office of Information Technology, contact
Vanessa Anderson at (202) 551-8800.
SUPPLEMENTARY INFORMATION: We are adopting an updated EDGAR Filer
Manual, Volume I and Volume II. The Filer Manual describes the
technical formatting requirements for the preparation and submission of
electronic filings through the EDGAR system.\1\ It also describes the
[[Page 13217]]
requirements for filing using EDGARLink Online and the Online Forms/XML
Web site.
---------------------------------------------------------------------------
\1\ We originally adopted the Filer Manual on April 1, 1993,
with an effective date of April 26, 1993. Release No. 33-6986 (April
1, 1993) [58 FR 18638]. We implemented the most recent update to the
Filer Manual on September 25, 2013. See Release No. 33-9457 (October
2, 2013) [78 FR 60684].
---------------------------------------------------------------------------
The revisions to the Filer Manual reflect changes within Volume I
entitled EDGAR Filer Manual, Volume I: ``General Information,'' Version
16 (March 2014) and Volume II entitled EDGAR Filer Manual, Volume II:
``EDGAR Filing,'' Version 26 (March 2014). The updated manual will be
incorporated by reference into the Code of Federal Regulations.
The Filer Manual contains all the technical specifications for
filers to submit filings using the EDGAR system. Filers must comply
with the applicable provisions of the Filer Manual in order to assure
the timely acceptance and processing of filings made in electronic
format.\2\ Filers may consult the Filer Manual in conjunction with our
rules governing mandated electronic filing when preparing documents for
electronic submission.\3\
---------------------------------------------------------------------------
\2\ See Rule 301 of Regulation S-T (17 CFR 232.301).
\3\ See Release No. 33-9457 in which we implemented EDGAR
Release 13.3. For additional history of Filer Manual rules, please
see the cites therein.
---------------------------------------------------------------------------
The EDGAR system will be upgraded to Release 14.0 on March 3, 2014
and will introduce the following changes: EDGAR will be updated to add
new submission form types MA, MA-A, MA/A, MA-I, MA-I/A, and MA-W on the
EDGAR Filing Web site. These submission form types can be accessed by
selecting the `File Municipal Advisor Forms' link available on the
EDGAR Filing Web site. Instructions to file the Municipal Advisor Forms
are included in two new sections of Chapter 9 (Preparing and
Transmitting Online Submissions) of the ``EDGAR Filer Manual, Volume
II: EDGAR Filing'' to guide filers through the filing process. See
Release No. 34-70462 \4\ for the compliance dates.
---------------------------------------------------------------------------
\4\ See Release No. 34-70462 (September 20, 2013) [78 FR 67467
(November 12, 2013)].
---------------------------------------------------------------------------
Submission form types 8-K, 8-K/A, 10-K, 10-K/A, 10-KT, 10-KT/A, 10-
D, 10-D/A, POS AM, 424B1, 424B2, 424B3, 424B4, 424B5, 424B7, and 424B8
will be updated to collect Depositor CIK, Sponsor CIK, ABS Asset Class,
and ABS Sub Asset Class information for filings where the primary
registrant CIK is designated as an Asset-Backed Securities issuing
entity (i.e., entities assigned the Standard Industrial Classification
Code 6189).
Submission form types 13F-HR/A will be updated to allow a future
date for the ``Date denied or on which confidential treatment expired''
field.
For EDGARLink Online application, recommended version for Firefox
browser is being changed from 3.5 to 17.0 or higher. For all EDGAR Web
sites, Microsoft Internet Explorer 7.0 or later is the recommended
browser. Additionally, minor documentation only corrections were made
to the Chapter 6, Interactive Data, sections 6.5.20 and 6.6.29.
Along with the adoption of the Filer Manual, we are amending Rule
301 of Regulation S-T to provide for the incorporation by reference
into the Code of Federal Regulations of today's revisions. This
incorporation by reference was approved by the Director of the Federal
Register in accordance with 5 U.S.C. 552(a) and 1 CFR Part 51.
You may obtain paper copies of the updated Filer Manual at the
following address: Public Reference Room, U.S. Securities and Exchange
Commission, 100 F Street NE., Room 1543, Washington, DC 20549, on
official business days between the hours of 10:00 a.m. and 3:00 p.m. We
will post electronic format copies on the Commission's Web site; the
address for the Filer Manual is https://www.sec.gov/info/edgar.shtml.
Since the Filer Manual and the corresponding rule changes relate
solely to agency procedures or practice, publication for notice and
comment is not required under the Administrative Procedure Act
(APA).\5\ It follows that the requirements of the Regulatory
Flexibility Act \6\ do not apply.
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\5\ 5 U.S.C. 553(b).
\6\ 5 U.S.C. 601-612.
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The effective date for the updated Filer Manual and the rule
amendments is March 10, 2014. In accordance with the APA,\7\ we find
that there is good cause to establish an effective date less than 30
days after publication of these rules. The EDGAR system upgrade to
Release 14.0 is scheduled to become available on March 3, 2014. The
Commission believes that establishing an effective date less than 30
days after publication of these rules is necessary to coordinate the
effectiveness of the updated Filer Manual with the system upgrade.
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\7\ 5 U.S.C. 553(d)(3).
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Statutory Basis
We are adopting the amendments to Regulation S-T under Sections 6,
7, 8, 10, and 19(a) of the Securities Act of 1933,\8\ Sections 3, 12,
13, 14, 15, 23, and 35A of the Securities Exchange Act of 1934,\9\
Section 319 of the Trust Indenture Act of 1939,\10\ and Sections 8, 30,
31, and 38 of the Investment Company Act of 1940.\11\
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\8\ 15 U.S.C. 77f, 77g, 77h, 77j, and 77s(a).
\9\ 15 U.S.C. 78c, 78l, 78m, 78n, 78o, 78w, and 78ll.
\10\ 15 U.S.C. 77sss.
\11\ 15 U.S.C. 80a-8, 80a-29, 80a-30, and 80a-37.
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List of Subjects in 17 CFR Part 232
Incorporation by reference, Reporting and recordkeeping
requirements, Securities.
Text of the Amendment
In accordance with the foregoing, Title 17, Chapter II of the Code
of Federal Regulations is amended as follows:
PART 232--REGULATION S-T--GENERAL RULES AND REGULATIONS FOR
ELECTRONIC FILINGS
0
1. The authority citation for Part 232 continues to read in part as
follows:
Authority: 15 U.S.C. 77f, 77g, 77h, 77j, 77s(a), 77z-3,
77sss(a), 78c(b), 78l, 78m, 78n, 78o(d), 78w(a), 78ll, 80a-6(c),
80a-8, 80a-29, 80a-30, 80a-37, and 7201 et seq.; and 18 U.S.C. 1350.
* * * * *
0
2. Section 232.301 is revised to read as follows:
Sec. 232.301 EDGAR Filer Manual.
Filers must prepare electronic filings in the manner prescribed by
the EDGAR Filer Manual, promulgated by the Commission, which sets out
the technical formatting requirements for electronic submissions. The
requirements for becoming an EDGAR Filer and updating company data are
set forth in the updated EDGAR Filer Manual, Volume I: ``General
Information,'' Version 16 (March 2014). The requirements for filing on
EDGAR are set forth in the updated EDGAR Filer Manual, Volume II:
``EDGAR Filing,'' Version 26 (March 2014). Additional provisions
applicable to Form N-SAR filers are set forth in the EDGAR Filer
Manual, Volume III: ``N-SAR Supplement,'' Version 2 (August 2011). All
of these provisions have been incorporated by reference into the Code
of Federal Regulations, which action was approved by the Director of
the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR Part
51. You must comply with these requirements in order for documents to
be timely received and accepted. You can obtain paper copies of the
EDGAR Filer Manual from the following address: Public Reference Room,
U.S. Securities and Exchange Commission, 100 F Street NE., Room 1543,
Washington, DC
[[Page 13218]]
20549, on official business days between the hours of 10:00 a.m. and
3:00 p.m. Electronic copies are available on the Commission's Web site.
The address for the Filer Manual is https://www.sec.gov/info/edgar.shtml. You can also inspect the document at the National Archives
and Records Administration (NARA). For information on the availability
of this material at NARA, call 202-741-6030, or go to: https://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html.
Dated: March 4, 2014.
By the Commission.
Elizabeth M. Murphy,
Secretary.
[FR Doc. 2014-05057 Filed 3-7-14; 8:45 am]
BILLING CODE 8011-01-P