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.

Urohealth Systems, Inc.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K980617 MODIFICATION TO REFLEX AEC LINEAR STAPLER/CUTTERGDW1998-04-09 View
510(k) K970107 INTUBATION ENDOSCOPE AND INTRODUCER SHEATHEOQ1997-11-18 View
510(k) K972510 PIVOTAL SCISSORGEI1997-11-13 View
↑