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Luxar Corp.

17 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM (K960475)Luxar Corp.1996-04-26
MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM (K953074)Luxar Corp.1995-08-28
MODIFIED LUXAR LX-20 FAMILY C02 LASER SYSTEM (K945888)Luxar Corp.1995-01-27
LUXAR MODEL LX-20 CO2 LASER (K904068)Luxar Corp.1991-04-15
ENDOGUIDE (R), MICROGUIDE (TM), FLEXIGUIDE (TM) (K903079)Luxar Corp.1990-10-04
FLEXIGUIDE(TM) CO2 LASER HOLLOW FLEXIBLE FIBER (K900066)Luxar Corp.1990-03-19
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (NEURO.) (K897040)Luxar Corp.1990-02-13
LUXAR MODEL LX-20 MINILASE CO2 LASER (K896478)Luxar Corp.1990-02-08
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (K896595)Luxar Corp.1990-01-09
LIST DERMATOLOGY/PLASTIC SURGERY AS USE ENDOGUIDE (K896619)Luxar Corp.1990-01-09
LISTING PODIATRY AS INTENDED USE FOR ENDOGUIDE (K896711)Luxar Corp.1990-01-09
LIST GENERAL SURGERY AS INTENDED USE FOR ENDOGUIDE (K896618)Luxar Corp.1990-01-09
LISTING ENT AS INTENDED USE FOR ENDOGUIDE (K896617)Luxar Corp.1990-01-09
ENDOGUIDE PRODUCT LINE: EX0120, EX0300 AND EX0400 (K895786)Luxar Corp.1989-10-27
MODIFIED ENDOGUIDE (K895559)Luxar Corp.1989-10-20
MODIFIED ENDOGUIDE (K893642)Luxar Corp.1989-07-14
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (K884459)Luxar Corp.1988-12-19

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