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Burr, Corneal, Battery-Powered

FDA product code HOG · 5 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.4070
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1984-03-19 – 1997-01-09
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