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.

Drape, Patient, Ophthalmic

FDA product code HMT · 7 cleared devices

Class 2 General, Plastic Surgery
Regulation
21 CFR 878.4370
Review panel
HO
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1983-04-06 – 1995-02-14
↑