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Lens, Contact (Orthokeratology)

FDA product code MUW · 6 cleared devices

Class 2 Ophthalmic
Regulation
21 CFR 886.5916
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1998-04-08 – 2019-01-09
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