Skytron, Div. the Kmw Group, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Skytron, Div. the Kmw Group, Inc. General & Plastic Surgery ✕
15 devices
Cleared
Jul 06, 2007
AURORA LED SERIES SURGICAL LIGHTS
General & Plastic Surgery
15d
Cleared
Nov 13, 2002
STELLAR SERIES SURGICAL LIGHTS WITH HERMES
General & Plastic Surgery
183d
Cleared
Nov 08, 2000
STELLAR
General & Plastic Surgery
90d
Cleared
Sep 08, 1999
MILLENNIUM GOLD
General & Plastic Surgery
79d
Cleared
Apr 03, 1995
SKYTRON SKYBOOM SERIES
General & Plastic Surgery
75d
Cleared
Jun 13, 1994
SKYTRON ELITE 3500 TABLE
General & Plastic Surgery
119d
Cleared
Feb 20, 1992
SKYTRON INFINITY SERIES SURGICAL LIGHTS
General & Plastic Surgery
87d
Cleared
Mar 19, 1990
SKYTRON UNIVERSE SERIES SURGICAL LIGHTS
General & Plastic Surgery
61d
Cleared
Feb 20, 1990
SKYTRON MODEL 1100 AND MODEL 142
General & Plastic Surgery
29d
Cleared
Sep 24, 1987
SKYTRON MODEL 130 SURGICAL TABLE
General & Plastic Surgery
31d
Cleared
Sep 12, 1985
SKYTRON ELITE 6000 & 6001 SURGICAL TABLES
General & Plastic Surgery
23d
Cleared
Sep 05, 1985
SKYTRON ELITE 300 SURGERY TABLE
General & Plastic Surgery
16d