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Device, Beam Limiting, X-Ray, Therapeutic

FDA product code KQA · 4 cleared devices

Class 2 Radiology
Regulation
21 CFR 892.5900
Review panel
RA
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1979-02-15 – 1992-06-05
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