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Device, Beam Limiting, Teletherapy, Radionuclide

FDA product code IWD · 1 cleared devices

Class 2 Radiology
Regulation
21 CFR 892.5750
Review panel
RA
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1997-05-28 – 1997-05-28
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