[Federal Register Volume 72, Number 184 (Monday, September 24, 2007)]
[Rules and Regulations]
[Pages 54207-54208]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E7-18743]


=======================================================================
-----------------------------------------------------------------------

NUCLEAR REGULATORY COMMISSION

10 CFR Parts 32 and 35

RIN 3150-AI14


Medical Use of Byproduct Material--Minor Corrections and 
Clarifications

AGENCY: Nuclear Regulatory Commission.

ACTION: Direct final rule: Confirmation of effective date.

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

SUMMARY: The Nuclear Regulatory Commission (NRC) is confirming the 
effective date of October 29, 2007, for the direct final rule that was 
published in the Federal Register on August 13, 2007 (72 FR 45147). 
This direct final rule amended the NRC's regulations to correct or 
clarify the rule language in several sections in the regulations that 
govern specific domestic licenses to manufacture or transfer certain 
items containing byproduct material and medical use of byproduct 
material.

DATES: The effective date of October 29, 2007 is confirmed for this 
direct final rule.

ADDRESSES: Documents related to this rulemaking, including comments 
received, may be examined at the NRC Public Document Room, Room O-1F23, 
11555 Rockville Pike, Rockville, MD 20852. These same documents are 
available electronically at the NRC's Electronic Reading Room at http://www.nrc.gov/NRC/reading-rm/adams.html. From this site, the public can 
gain entry into ADAMS, which provides text and image files of NRC's 
public documents. If you do not have access to ADAMS or if there are 
problems in accessing the documents located in ADAMS, contact the PDR 
Reference staff at 1-800-397-4209, 301-415-4737.

FOR FURTHER INFORMATION CONTACT: Edward M. Lohr, Office of Federal and 
State Materials and Environmental Management Programs, U.S. Nuclear 
Regulatory Commission, Washington, DC 20555, telephone (301) 415-0253 
(e-mail: [email protected]).

SUPPLEMENTARY INFORMATION: On August 13, 2007 (72 FR 45147), the NRC 
published in the Federal Register a direct final rule amending its 
regulations in 10 CFR Parts 32 and 35 to correct or clarify the rule 
language in several sections in the regulations that

[[Page 54208]]

govern specific domestic licenses to manufacture or transfer certain 
items containing byproduct material and medical use of byproduct 
material. In the direct final rule, NRC stated that if no significant 
adverse comments were received, the direct final rule would become 
final on October 29, 2007. The NRC did not receive any comments that 
warranted withdrawal of the direct final rule. Therefore, this rule 
will become effective as scheduled.

    Dated at Rockville, Maryland, this 18th day of September, 2007.

    For the Nuclear Regulatory Commission.
Michael T. Lesar,
Chief, Rulemaking, Directives and Editing Branch, Division of 
Administrative Services, Office of Administration.
[FR Doc. E7-18743 Filed 9-21-07; 8:45 am]
BILLING CODE 7590-01-P