Minnesota Laser Corp.

12 FDA 510(k) medical device clearances.

Top product codes for Minnesota Laser Corp.

GEX — General, Plastic Surgery 5 devices
EWG — Ear, Nose, Throat 2 devices
HHR — Obstetrics/Gynecology 2 devices
LNK — General, Plastic Surgery 2 devices
LLO — Ear, Nose, Throat 1 device

Recent clearances by Minnesota Laser Corp.

K874253 — ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA. LNK · 1988-07-12
K874255 — ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. LNK · 1988-07-12
K874254 — ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS LLO · 1988-03-04
K854468 — PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC GEX · 1986-06-20
K854473 — PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGIC GEX · 1986-06-20
K854471 — PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T EWG · 1986-02-13
K854469 — PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG GEX · 1986-02-11
K854472 — PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG GEX · 1986-02-11
K854470 — PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGI HHR · 1986-02-07
K852694 — PORTALASE 200 CARBON SURGICAL LASER SYSTEM HHR · 1985-09-30
K852696 — FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGY GEX · 1985-09-19
K852695 — FOR USE IN EAR; NOSE & THROAT MICROSURGERY EWG · 1985-08-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.