Medical Device Manufacturer · US , Minneapolis , MN

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

12 submissions · 11 cleared · Since 1985

Total

Cleared

Denied

Minnesota Laser Corp. has 11 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 11 cleared submissions from 1985 to 1988. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Minnesota Laser Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Minnesota Laser Corp.

12 devices

1-12 of 12

Cleared Jul 12, 1988

ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.

K874253 · LNK

Gastroenterology & Urology · 266d

Cleared Jul 12, 1988

ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.

K874255 · LNK

Gastroenterology & Urology · 266d

Cleared Mar 04, 1988

ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS

K874254 · LLO

Anesthesiology · 136d

Cleared Jun 20, 1986

PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC

K854468 · GEX

General & Plastic Surgery · 226d

Cleared Jun 20, 1986

PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGIC

K854473 · GEX

General & Plastic Surgery · 226d

Cleared Feb 13, 1986

PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T

K854471 · EWG

Ear, Nose, Throat · 99d

Cleared Feb 11, 1986

PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG

K854469 · GEX

General & Plastic Surgery · 97d

Cleared Feb 11, 1986

PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG

K854472 · GEX

General & Plastic Surgery · 97d

Cleared Feb 07, 1986

PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGI

K854470 · HHR

Obstetrics & Gynecology · 93d

Cleared Sep 30, 1985

PORTALASE 200 CARBON SURGICAL LASER SYSTEM

K852694 · HHR

Obstetrics & Gynecology · 96d

Cleared Sep 19, 1985

FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGY

K852696 · GEX

General & Plastic Surgery · 85d

Cleared Aug 30, 1985

FOR USE IN EAR

K852695 · EWG

Ear, Nose, Throat · 65d

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

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