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Retinoscope, Ac-Powered

FDA product code HKL · 6 cleared devices

Class 2 Ophthalmic
Regulation
21 CFR 886.1780
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1980-03-10 – 2000-07-07
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