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Screen, Tangent, Projection, Ac-Powered

FDA product code HOK · 1 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.1810
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1992-01-23 – 1992-01-23
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