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Lens, Guide, Intraocular

FDA product code KYB · 38 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.4300
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1979-08-03 – 2008-10-23
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