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. General & Plastic Surgery ✕

5 devices

1-5 of 5

Cleared Jun 20, 1986

PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC

General & Plastic Surgery · 226d

Cleared Jun 20, 1986

PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGIC

General & Plastic Surgery · 226d

Cleared Feb 11, 1986

PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG

General & Plastic Surgery · 97d

Cleared Feb 11, 1986

PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG

General & Plastic Surgery · 97d

Cleared Sep 19, 1985

FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGY

General & Plastic Surgery · 85d