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Goniometer, Nonpowered

FDA product code KQW · 13 cleared devices

Class 1 Orthopedic
Regulation
21 CFR 888.1520
Review panel
NE
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1976-09-08 – 1993-08-02
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