Mnlase, Inc.
Minneapolis, MN, US
Mnlase, Inc. appears in FDA device records in Minneapolis, MN. FDA records list 22 510(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
- 22
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 22 510(k) clearances for Mnlase, Inc. between 1992 and 1994. The busiest year on record is 1994, with 16. The most recent is 1994, with 16.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1992 | 6 |
| 1994 | 16 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K944630 | MODEL 230-SAS LASER DELIVERY PROBE | GEX | Substantially Equivalent | |
| K944629 | MODEL 230-SAC LASER DELIVERY PROBE | GEX | Substantially Equivalent | |
| K944628 | MODEL 220-SS LASER DELIVERY PROBE | GEX | Substantially Equivalent | |
| K944627 | MODEL 220-SC CURVED ENDOPHOTOCOAGULATOR LASER | GEX | Substantially Equivalent | |
| K944626 | MODEL 210-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER | GEX | Substantially Equivalent | |
| K944625 | MODEL 210-AC ASPIRATING ENDOPHOTOCOAGULATOR LASER | GEX | Substantially Equivalent | |
| K944471 | STRAIGHT ENDOPHOTOCOAGULATOR LASER PROBE | GEX | Substantially Equivalent | |
| K944470 | CURVED ENDOPHOTOCOAGULATOR LASER PROBE | GEX | Substantially Equivalent | |
| K944632 | MODEL 120-SS LASER DELIVERY PROBE | GEX | Substantially Equivalent | |
| K944631 | MODEL 120-SC LASER DELIVERY PROBE | GEX | Substantially Equivalent | |
| K944624 | MODEL 130-SAC ASPIRATING ENDOPHOTOCOAGULATOR LASER | GEX | Substantially Equivalent | |
| K944623 | MODEL 130-SAS ASPIRATING ENDOPHOTOCOAGULATOR LASER | GEX | Substantially Equivalent | |
| K944622 | MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER | GEX | Substantially Equivalent | |
| K944621 | MODEL 110-AC ASPIRATING ENDOPHOTOCOAGULATOR LASER | GEX | Substantially Equivalent | |
| K944472 | CURVD ENDOPHOTOCOGULATOR LASER PROBE | GEX | Substantially Equivalent | |
| K944282 | LASER DELIVERY PROBE | GEX | Substantially Equivalent | |
| K921570 | ORS-300 | JRM | Substantially Equivalent | |
| K921569 | ORS-200 | JRM | Substantially Equivalent | |
| K921568 | ORS-100 | JRM | Substantially Equivalent | |
| K921633 | ORS-2000 SERIES | LHC | Substantially Equivalent | |
| K915085 | DL100 C02 SURGICAL LASER SYSTEM | GEX | Substantially Equivalent | |
| K915427 | ORS-1000 | JRM | 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