Minnesota Laser Corp.
Minnesota Laser Corp. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1988.
Top product codes for Minnesota Laser Corp.
Recent clearances by Minnesota Laser Corp.
- K874253 — ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.
- K874255 — ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.
- K874254 — ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS
- K854468 — PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC
- K854473 — PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGIC
- K854471 — PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T
- K854469 — PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG
- K854472 — PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG
- K854470 — PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGI
- K852694 — PORTALASE 200 CARBON SURGICAL LASER SYSTEM
- K852696 — FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGY
- K852695 — FOR USE IN EAR; NOSE & THROAT MICROSURGERY
Data sourced from openFDA. This site is unofficial and independent of the FDA.