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Instrument, Cast Removal, Ac-Powered

FDA product code LGH · 9 cleared devices

Class 1 Orthopedic
Regulation
21 CFR 888.5960
Review panel
OR
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1982-03-02 – 1994-01-28
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