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Inserter/Remover Contact Lens

FDA product code KYE · 12 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.5420
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1978-05-17 – 1987-08-10
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