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Prism, Gonioscopic

FDA product code HKS · 9 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.1660
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1983-02-07 – 1994-04-01
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