Service of Process on Manufacturers; Manufacturers Importing Electronic Products Into the United States; Agent Designation; Change of Address, 18234 [2013-06864]

Download as PDF 18234 Federal Register / Vol. 78, No. 58 / Tuesday, March 26, 2013 / Rules and Regulations PART 870—CARDIOVASCULAR DEVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES PART 1005—IMPORTATION OF ELECTRONIC PRODUCTS 2. The authority citation for 21 CFR part 870 continues to read as follows: Food and Drug Administration ■ ■ Authority: 21 U.S.C. 351, 360, 360c, 360e, 360j, 371. 3. Amend § 870.3600 by revising the second sentence in paragraph (a) to read as follows: 21 CFR Part 1005 Authority: 21 U.S.C. 360ii, 360mm. [Docket No. FDA–2007–N–0091; (formerly 2007N–0104)] ■ § 870.3600 generator. External pacemaker pulse (a) Identification. * * * This device, which is used outside the body, is used as a temporary substitute for the heart’s intrinsic pacing system until a permanent pacemaker can be implanted, or to control irregular heartbeats in patients following cardiac surgery or a myocardial infarction. * * * * * * * * ■ 4. Amend § 870.5300 by revising the section heading to read as follows: § 870.5300 paddles). DC-defibrillator (including * * * * * PART 882—NEUROLOGICAL DEVICES 5. The authority citation for 21 CFR part 882 continues to read as follows: ■ Authority: 21 U.S.C. 351, 360, 360c, 360e, 360j, 371. 6. Amend § 882.5870 by revising the second sentence in paragraph (a) to read as follows: ■ § 882.5870 Implanted peripheral nerve stimulator for pain relief. (a) Identification. * * * The stimulator consists of an implanted receiver with electrodes that are placed around a peripheral nerve and an external transmitter for transmitting the stimulating pulses across the patient’s skin to the implanted receiver. * * * * * PART 886—OPHTHALMIC DEVICES 7. The authority citation for 21 CFR part 886 continues to read as follows: ■ Authority: 21 U.S.C. 351, 360, 360c, 360e, 360j, 371. 8. Amend § 886.1120 by revising the section heading to read as follows: ■ tkelley on DSK3SPTVN1PROD with RULES § 886.1120 Ophthalmic camera. * * * * * Dated: March 20, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013–06826 Filed 3–25–13; 8:45 am] BILLING CODE 4160–01–P VerDate Mar<15>2010 16:42 Mar 25, 2013 Jkt 229001 1. The authority citation for 21 CFR part 1005 continues to read as follows: § 1005.25 [Amended] 2. Section 1005.25(b) is amended by removing ‘‘Center for Devices and Radiological Health (HFZ–240), 9200 Corporate Blvd., Rockville, MD 20850’’ and by adding in its place ‘‘Center for Devices and Radiological Health, 10903 New Hampshire Ave., Document Mail Center—WO66–G609, Silver Spring, MD 20993–0002’’. ■ Service of Process on Manufacturers; Manufacturers Importing Electronic Products Into the United States; Agent Designation; Change of Address AGENCY: Food and Drug Administration, HHS. Final rule; technical amendment. ACTION: The Food and Drug Administration (FDA) is amending a final rule that appeared in the Federal Register of April 9, 2007 (72 FR 17397 at 17401) to reflect changes to the Center for Devices and Radiological Health’s address. This action is editorial in nature and is intended to improve the accuracy of the Agency’s regulations. DATES: This rule is effective March 26, 2013 FOR FURTHER INFORMATION CONTACT: Prince P. Kangoma, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave. Bldg. 66, rm. G628B, 301–796– 6627, FAX: 301–595–7850, email: Prince.Kangoma@fda.hhs.gov. SUMMARY: FDA is making technical amendments in the Agency’s regulations under 21 CFR 1005.25(b) as a result of an office relocation. The former address was 9200 Corporate Blvd., Rockville, MD 20850. The new address is 10903 New Hampshire Ave., Silver Spring, MD 20993–0002. Designation of agent by manufacturers of electronic products offering such products for importation into the United States must be addressed to the Center for Devices and Radiological Health, Document Mail Center—WO66–G609. Publication of this document constitutes final action of these changes under the Administrative Procedures Act (5 U.S.C. 553). Notice and public procedures are unnecessary because FDA is merely updating nonsubstantive content. SUPPLEMENTARY INFORMATION: List of Subjects in 21 CFR Part 1005 Administrative practice and procedure; Electronic product; Imports; Radiation protection; Surety bonds. Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs, 21 CFR part 1005 is amended as follows: PO 00000 Frm 00014 Fmt 4700 Sfmt 4700 Dated: March 20, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013–06864 Filed 3–25–13; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HOUSING AND URBAN DEVELOPMENT 24 CFR Part 970 Demolition or Disposition of Public Housing Projects CFR Correction In Title 24 of the Code of Federal Regulations, Parts 700 to 1699, revised as of April 1, 2012, on page 490, in § 970.27, redesignate paragraph (c) introductory text as paragraph (b). ■ [FR Doc. 2013–07091 Filed 3–25–13; 8:45 am] BILLING CODE 1505–01–D DEPARTMENT OF THE TREASURY Internal Revenue Service 26 CFR Part 1 Section 482: Methods To Determine Taxable Income in Connection With a Cost Sharing Arrangement CFR Correction In Title 26 of the Code of Federal Regulations, Part 1 (§§ 1.441 to 1.500), revised as of April 1, 2012, on page 604, in § 1.482–1, in paragraph (c)(1), before the last sentence, reinstate the following sentence: ■ § 1.482–1 Allocation of income and deductions among taxpayers. * E:\FR\FM\26MRR1.SGM * * 26MRR1 * *

Agencies

[Federal Register Volume 78, Number 58 (Tuesday, March 26, 2013)]
[Rules and Regulations]
[Page 18234]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-06864]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 1005

[Docket No. FDA-2007-N-0091; (formerly 2007N-0104)]


Service of Process on Manufacturers; Manufacturers Importing 
Electronic Products Into the United States; Agent Designation; Change 
of Address

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule; technical amendment.

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

SUMMARY: The Food and Drug Administration (FDA) is amending a final 
rule that appeared in the Federal Register of April 9, 2007 (72 FR 
17397 at 17401) to reflect changes to the Center for Devices and 
Radiological Health's address. This action is editorial in nature and 
is intended to improve the accuracy of the Agency's regulations.

DATES: This rule is effective March 26, 2013

FOR FURTHER INFORMATION CONTACT: Prince P. Kangoma, Center for Devices 
and Radiological Health, Food and Drug Administration, 10903 New 
Hampshire Ave. Bldg. 66, rm. G628B, 301-796-6627, FAX: 301-595-7850, 
email: Prince.Kangoma@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: FDA is making technical amendments in the 
Agency's regulations under 21 CFR 1005.25(b) as a result of an office 
relocation. The former address was 9200 Corporate Blvd., Rockville, MD 
20850. The new address is 10903 New Hampshire Ave., Silver Spring, MD 
20993-0002. Designation of agent by manufacturers of electronic 
products offering such products for importation into the United States 
must be addressed to the Center for Devices and Radiological Health, 
Document Mail Center--WO66-G609. Publication of this document 
constitutes final action of these changes under the Administrative 
Procedures Act (5 U.S.C. 553). Notice and public procedures are 
unnecessary because FDA is merely updating nonsubstantive content.

List of Subjects in 21 CFR Part 1005

    Administrative practice and procedure; Electronic product; Imports; 
Radiation protection; Surety bonds.

    Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
authority delegated to the Commissioner of Food and Drugs, 21 CFR part 
1005 is amended as follows:

PART 1005--IMPORTATION OF ELECTRONIC PRODUCTS

0
1. The authority citation for 21 CFR part 1005 continues to read as 
follows:

    Authority:  21 U.S.C. 360ii, 360mm.


Sec.  1005.25  [Amended]

0
2. Section 1005.25(b) is amended by removing ``Center for Devices and 
Radiological Health (HFZ-240), 9200 Corporate Blvd., Rockville, MD 
20850'' and by adding in its place ``Center for Devices and 
Radiological Health, 10903 New Hampshire Ave., Document Mail Center--
WO66-G609, Silver Spring, MD 20993-0002''.

    Dated: March 20, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-06864 Filed 3-25-13; 8:45 am]
BILLING CODE 4160-01-P
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