Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Keratoscope, Ac-Powered

FDA product code HLQ · 29 cleared devices

Class 1 Ophthalmic
Regulation
21 CFR 886.1350
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1979-02-12 – 2001-03-09
↑