Medical Device Manufacturer · US , Minneapolis , MN

Minnesota Laser Corp. - FDA 510(k) Cleared Devices

12 submissions · 11 cleared · Since 1985

12

Total

11

Cleared

0

Denied

FDA 510(k) Regulatory Record - Minnesota Laser Corp. Obstetrics & Gynecology ✕

2 devices

1-2 of 2

Cleared Feb 07, 1986

PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGI

Obstetrics & Gynecology · 93d

Cleared Sep 30, 1985

PORTALASE 200 CARBON SURGICAL LASER SYSTEM

Obstetrics & Gynecology · 96d