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Phantom, Anthropomorphic, Radiographic

FDA product code IXG · 4 cleared devices

Class 1 Radiology
Regulation
21 CFR 892.1950
Review panel
RA
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
Yes
Clearance span
1984-02-21 – 1991-09-19
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