Medical Device Manufacturer · US , Dallas , TX

Lasermatic, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1988

8

Total

8

Cleared

0

Denied

Lasermatic, Inc. has 8 FDA 510(k) cleared medical devices. Based in Dallas, US.

Historical record: 8 cleared submissions from 1988 to 1991. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Lasermatic, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lasermatic, Inc.

8 devices

1-8 of 8

Cleared Feb 19, 1991

LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEM

General & Plastic Surgery · 217d

Cleared Jun 27, 1990

MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33

General & Plastic Surgery · 79d

Cleared Jun 08, 1989

COMBOLASER MODEL 5050

General & Plastic Surgery · 31d

Cleared Aug 22, 1988

MODEL 5050 SURGILASER FOR OB-GYN USE

Obstetrics & Gynecology · 466d

Cleared Mar 25, 1988

MODEL 5050 SURGILASER FOR UROLOGY USE

Gastroenterology & Urology · 311d

Cleared Mar 25, 1988

MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE

Gastroenterology & Urology · 311d

Cleared Jan 22, 1988

MODEL 5050 SURGILASER FOR PULMONARY USE

Anesthesiology · 253d

Cleared Jan 22, 1988

MODEL 5050 SURGILASER FOR NEUROSURGERY USE

General & Plastic Surgery · 248d