Luxar Corp.
Luxar Corp. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1996.
Top product codes for Luxar Corp.
Recent clearances by Luxar Corp.
- K960475 — MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM
- K953074 — MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM
- K945888 — MODIFIED LUXAR LX-20 FAMILY C02 LASER SYSTEM
- K904068 — LUXAR MODEL LX-20 CO2 LASER
- K903079 — ENDOGUIDE (R), MICROGUIDE (TM), FLEXIGUIDE (TM)
- K900066 — FLEXIGUIDE(TM) CO2 LASER HOLLOW FLEXIBLE FIBER
- K897040 — LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (NEURO.)
- K896478 — LUXAR MODEL LX-20 MINILASE CO2 LASER
- K896595 — LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE
- K896617 — LISTING ENT AS INTENDED USE FOR ENDOGUIDE
- K896618 — LIST GENERAL SURGERY AS INTENDED USE FOR ENDOGUIDE
- K896619 — LIST DERMATOLOGY/PLASTIC SURGERY AS USE ENDOGUIDE
- K896711 — LISTING PODIATRY AS INTENDED USE FOR ENDOGUIDE
- K895786 — ENDOGUIDE PRODUCT LINE: EX0120, EX0300 AND EX0400
- K895559 — MODIFIED ENDOGUIDE
- K893642 — MODIFIED ENDOGUIDE
- K884459 — LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE
Data sourced from openFDA. This site is unofficial and independent of the FDA.