Minnesota Laser Corp.
Minneapolis, MN, US
Minnesota Laser Corp. appears in FDA device records in Minneapolis, MN. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Minnesota Laser Corp. between 1985 and 1988. The busiest year on record is 1986, with 6. The most recent is 1988, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 3 |
| 1986 | 6 |
| 1988 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K874255 | ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. | LNK | Substantially Equivalent | |
| K874253 | ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA. | LNK | Substantially Equivalent | |
| K874254 | ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS | LLO | Substantially Equivalent | |
| K854473 | PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGIC | GEX | Substantially Equivalent | |
| K854468 | PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC | GEX | Substantially Equivalent | |
| K854471 | PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T | EWG | Substantially Equivalent | |
| K854472 | PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG | GEX | Substantially Equivalent | |
| K854469 | PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG | GEX | Substantially Equivalent | |
| K854470 | PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGI | HHR | Substantially Equivalent | |
| K852694 | PORTALASE 200 CARBON SURGICAL LASER SYSTEM | HHR | Substantially Equivalent for Some Indications | |
| K852696 | FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGY | GEX | Substantially Equivalent | |
| K852695 | FOR USE IN EAR; NOSE & THROAT MICROSURGERY | EWG | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain