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System, Imaging, X-Ray, Electrostatic

FDA product code IXK · 14 cleared devices

Class 2 Radiology
Regulation
21 CFR 892.1630
Review panel
RA
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1976-11-24 – 2011-04-29
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