Luxar Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Luxar Corp. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Luxar Corp. has 17 FDA 510(k) cleared general & plastic surgery devices. Based in Bothell, US.
Historical record: 17 cleared submissions from 1988 to 1996.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Luxar Corp.
17 devices
Cleared
Apr 26, 1996
MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM
General & Plastic Surgery
85d
Cleared
Aug 28, 1995
MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM
General & Plastic Surgery
59d
Cleared
Jan 27, 1995
MODIFIED LUXAR LX-20 FAMILY C02 LASER SYSTEM
General & Plastic Surgery
57d
Cleared
Apr 15, 1991
LUXAR MODEL LX-20 CO2 LASER
General & Plastic Surgery
227d
Cleared
Oct 04, 1990
ENDOGUIDE (R), MICROGUIDE (TM), FLEXIGUIDE (TM)
General & Plastic Surgery
84d
Cleared
Mar 19, 1990
FLEXIGUIDE(TM) CO2 LASER HOLLOW FLEXIBLE FIBER
General & Plastic Surgery
74d
Cleared
Feb 13, 1990
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (NEURO.)
General & Plastic Surgery
57d
Cleared
Feb 08, 1990
LUXAR MODEL LX-20 MINILASE CO2 LASER
General & Plastic Surgery
87d
Cleared
Jan 09, 1990
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE
General & Plastic Surgery
49d
Cleared
Jan 09, 1990
LISTING ENT AS INTENDED USE FOR ENDOGUIDE
General & Plastic Surgery
49d
Cleared
Jan 09, 1990
LIST GENERAL SURGERY AS INTENDED USE FOR ENDOGUIDE
General & Plastic Surgery
49d
Cleared
Jan 09, 1990
LIST DERMATOLOGY/PLASTIC SURGERY AS USE ENDOGUIDE
General & Plastic Surgery
49d