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Keratome, Battery-Powered

FDA product code HMY · 12 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.4370
Review panel
OP
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1978-10-11 – 2004-03-31
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