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.

Lasermatic, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K903131 LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEMGEX1991-02-19 View
510(k) K901638 MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33GEX1990-06-27 View
510(k) K893529 COMBOLASER MODEL 5050GEX1989-06-08 View
510(k) K871875 MODEL 5050 SURGILASER FOR OB-GYN USEHHR1988-08-22 View
510(k) K871934 MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USELNK1988-03-25 View
510(k) K871932 MODEL 5050 SURGILASER FOR UROLOGY USELNK1988-03-25 View
510(k) K871933 MODEL 5050 SURGILASER FOR NEUROSURGERY USEGEX1988-01-22 View
510(k) K871876 MODEL 5050 SURGILASER FOR PULMONARY USELLO1988-01-22 View
↑