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Clamp, Eyelid, Ophthalmic

FDA product code HOD · 3 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.4350
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1983-06-03 – 1993-04-14
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