Burton Medical Products Corp. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
FDA 510(k) Regulatory Record - Burton Medical Products Corp. General & Plastic Surgery ✕
8 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
Jan 24, 1986
PL EXAM LIGHT
General & Plastic Surgery
14d