Lasermatic, Inc.
Lasermatic, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1991.
Top product codes for Lasermatic, Inc.
Recent clearances by Lasermatic, Inc.
- K903131 — LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEM
- K901638 — MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33
- K893529 — COMBOLASER MODEL 5050
- K871875 — MODEL 5050 SURGILASER FOR OB-GYN USE
- K871932 — MODEL 5050 SURGILASER FOR UROLOGY USE
- K871934 — MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE
- K871876 — MODEL 5050 SURGILASER FOR PULMONARY USE
- K871933 — MODEL 5050 SURGILASER FOR NEUROSURGERY USE
Data sourced from openFDA. This site is unofficial and independent of the FDA.