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.

Gynecare, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K992901 GYNECARE VERSAPOINT G-VAP ELECTRODEHIH2000-01-18 View
510(k) K982738 VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA)HIH1999-03-01 View
510(k) K962482 SCUBA SYSTEMHIH1996-11-01 View
↑