Luxar Corp.
Bothell, WA, US
Luxar Corp. appears in FDA device records in Bothell, WA. FDA records list 16 510(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
- 16
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 16 510(k) clearances for Luxar Corp. between 1988 and 1995. The busiest year on record is 1990, with 9. The most recent is 1995, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1989 | 3 |
| 1990 | 9 |
| 1991 | 1 |
| 1995 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K953074 | MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM | GEX | Substantially Equivalent | |
| K945888 | MODIFIED LUXAR LX-20 FAMILY C02 LASER SYSTEM | GEX | Substantially Equivalent | |
| K904068 | LUXAR MODEL LX-20 CO2 LASER | GEX | Substantially Equivalent | |
| K903079 | ENDOGUIDE (R), MICROGUIDE (TM), FLEXIGUIDE (TM) | GEX | Substantially Equivalent | |
| K900066 | FLEXIGUIDE(TM) CO2 LASER HOLLOW FLEXIBLE FIBER | GEX | Substantially Equivalent | |
| K897040 | LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (NEURO.) | GEX | Substantially Equivalent | |
| K896478 | LUXAR MODEL LX-20 MINILASE CO2 LASER | GEX | Substantially Equivalent | |
| K896711 | LISTING PODIATRY AS INTENDED USE FOR ENDOGUIDE | GEX | Substantially Equivalent | |
| K896619 | LIST DERMATOLOGY/PLASTIC SURGERY AS USE ENDOGUIDE | GEX | Substantially Equivalent | |
| K896618 | LIST GENERAL SURGERY AS INTENDED USE FOR ENDOGUIDE | GEX | Substantially Equivalent | |
| K896617 | LISTING ENT AS INTENDED USE FOR ENDOGUIDE | GEX | Substantially Equivalent | |
| K896595 | LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE | GEX | Substantially Equivalent | |
| K895786 | ENDOGUIDE PRODUCT LINE: EX0120, EX0300 AND EX0400 | GEX | Substantially Equivalent | |
| K895559 | MODIFIED ENDOGUIDE | GEX | Substantially Equivalent | |
| K893642 | MODIFIED ENDOGUIDE | GEX | Substantially Equivalent | |
| K884459 | LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE | GEX | 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