Burton Medical Products Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Burton Medical Products Corp. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Burton Medical Products Corp. has 15 FDA 510(k) cleared medical devices. Based in Van Nuys, US.
Historical record: 15 cleared submissions from 1985 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Burton Medical Products Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Burton Medical Products Corp.
15 devices
Cleared
Sep 30, 2010
AIM 200, MAJOR SURGICAL LIGHT
General & Plastic Surgery
119d
Cleared
Dec 01, 2004
OUTPATIENT III MINOR SURGERY LIGHT
General & Plastic Surgery
90d
Cleared
May 25, 2000
VISIONARY 2000
General & Plastic Surgery
90d
Cleared
Nov 13, 1996
GENIE' SINGLE CEILING AND DOUBLE CEILING
General & Plastic Surgery
71d
Cleared
Aug 22, 1996
GENIE
General & Plastic Surgery
101d
Cleared
Jun 27, 1994
SATURN LIGHT
General & Plastic Surgery
248d
Cleared
Jun 23, 1994
GENESIS
General & Plastic Surgery
23d
Cleared
Apr 26, 1994
WAVE FLUORESCENT MAGNIFIER
General Hospital
126d
Cleared
Aug 20, 1993
HALUX TASKLIGHT
General Hospital
140d
Cleared
Jul 19, 1990
LIGHT, HEAD, EXAMINATION
General Hospital
98d
Cleared
Aug 15, 1989
MODEL 0183010, PEARL MEDICAL EXAM LIGHT
General Hospital
85d
Cleared
Aug 15, 1989
MODEL 0450000, OPAL MEDICAL EXAM LIGHT
General Hospital
85d
Cleared
Apr 18, 1986
BASIC LIGHT
General Hospital
11d
Cleared
Jan 24, 1986
PL EXAM LIGHT
General & Plastic Surgery
14d
Cleared
May 13, 1985
MEDICAL EXAMINATION LIGHTS
General Hospital
14d