[Code of Federal Regulations]
[Title 10, Volume 1]
[Revised as of January 1, 2001]
From the U.S. Government Printing Office via GPO Access
[CITE: 10CFR35.12]

[Page 556]
 
                            TITLE 10--ENERGY
 
                CHAPTER I--NUCLEAR REGULATORY COMMISSION
 
PART 35--MEDICAL USE OF BYPRODUCT MATERIAL--Table of Contents
 
                     Subpart A--General Information
 
Sec. 35.12  Application for license, amendment, or renewal.

    (a) If the application is for medical use sited in a medical 
institution, only the institution's management may apply. If the 
application is for medical use not sited in a medical institution, any 
person may apply.
    (b) An application for a license for medical use of byproduct 
material as described in Secs. 35.100, 35.200, 35.300, 35.400, and 
35.500 of this part must be made by filing an original and one copy of 
Form NRC-313, ``Application for Materials License.'' For guidance in 
completing the form, refer to the instructions in the most current 
versions of the appropriate Regulatory Guides. A request for a license 
amendment or renewal may be submitted as an original and one copy in 
letter format.
    (c) An application for a license for medical use of byproduct 
material as described in Sec. 35.600 of this part must be made by filing 
an original and one copy of Form NRC-313. For guidance in completing the 
form, refer to the instructions in the most current version of the 
appropriate Regulatory Guide. A request for a license amendment or 
renewal may be submitted as an original and one copy in letter format.
    (d) For copies of regulatory guides, application forms, or to submit 
an application or an amendment request, refer to Sec. 30.6 of this 
chapter.
    (e) An applicant that satisfies the requirements specified in 10 CFR 
33.13 may apply for a Type A specific license of broad scope.

[51 FR 36951, Oct. 16, 1986, as amended at 59 FR 61782, Dec. 2, 1994]