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Device, Measuring, Lens Radius, Ophthalmic

FDA product code HLF · 3 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.1430
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1983-01-08 – 1993-08-09
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