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Device, Beam Limiting, X-Ray, Diagnostic

FDA product code KPW · 16 cleared devices

Class 2 Radiology
Regulation
21 CFR 892.1610
Review panel
RA
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1977-02-28 – 2010-01-12
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