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Spectacle, Operating (Loupe), Ophthalmic

FDA product code HOH · 3 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.4770
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
Yes
Clearance span
1981-04-23 – 1994-01-25
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