Reliant Laser Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reliant Laser Corp. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Reliant Laser Corp. has 3 FDA 510(k) cleared medical devices. Based in Foster City, US.
Historical record: 3 cleared submissions from 1992 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Reliant Laser Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Reliant Laser Corp.
3 devices
Cleared
Jun 15, 1995
ACUTOME(R) 150 MULTI-WAVELENGTH COLOR-CORRECTED(TM) LASER HANDPIECE
General & Plastic Surgery
147d
Cleared
Nov 14, 1994
ACUTOME 2000 COLOR-CORRECTED LAPAROSCOPIC C02 LASER COUPLER AND SLEEVES
General & Plastic Surgery
150d
Cleared
May 21, 1992
UNIMAX MODEL 2000 COLOR-CORRECTED MICROSPOT CO2
General & Plastic Surgery
87d