Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Minnesota Laser Corp. — Predicate Candidate Screening

12 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

99 daysmedian FDA review time
266 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K874255ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.Minnesota Laser Corp.1988-07-122660
K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.Minnesota Laser Corp.1988-07-122660
K874254ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONSMinnesota Laser Corp.1988-03-041360
K854468PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGICMinnesota Laser Corp.1986-06-202260
K854473PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGICMinnesota Laser Corp.1986-06-202260
K854471PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/TMinnesota Laser Corp.1986-02-13990
K854472PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOGMinnesota Laser Corp.1986-02-11970
K854469PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOGMinnesota Laser Corp.1986-02-11970
K854470PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGIMinnesota Laser Corp.1986-02-07930
K852694PORTALASE 200 CARBON SURGICAL LASER SYSTEMMinnesota Laser Corp.1985-09-30960
K852696FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGYMinnesota Laser Corp.1985-09-19850
K852695FOR USE IN EAR; NOSE & THROAT MICROSURGERYMinnesota Laser Corp.1985-08-30650

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda