Part 35 — Medical Use of Byproduct Material
- Subpt. A General Information §§35.1 to 35.19
- Subpt. B General Administrative Requirements §§35.24 to 35.59
- Subpt. C General Technical Requirements §§35.60 to 35.92
- Subpt. D Unsealed Byproduct Material—Written Directive Not Required §§35.100 to 35.290
- Subpt. E Unsealed Byproduct Material—Written Directive Required §§35.300 to 35.396
- Subpt. F Manual Brachytherapy §§35.400 to 35.491
- Subpt. G Sealed Sources for Diagnosis §§35.500 to 35.590
- Subpt. H Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units §§35.600 to 35.690
- Subpt. I-J Subparts I-J [Reserved]
- Subpt. K Other Medical Uses of Byproduct Material or Radiation From Byproduct Material §35.1000
- Subpt. L Records §§35.2024 to 35.2655
- Subpt. M Reports §§35.3045 to 35.3204
- Subpt. N Enforcement §§35.4001 to 35.4002