Skytron, Div. the Kmw Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Skytron, Div. the Kmw Group, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Skytron, Div. the Kmw Group, Inc. has 19 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1981 to 2007.
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 - Skytron, Div. the Kmw Group, Inc.
19 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 10, 1994
SKYTRON EXAM LIGHT
General Hospital
203d
Cleared
Jul 27, 1993
SKYTRON LIFE ISLAND 21
General Hospital
238d
Cleared
Feb 20, 1992
SKYTRON INFINITY SERIES SURGICAL LIGHTS
General & Plastic Surgery
87d
Cleared
Sep 04, 1990
SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI
Neurology
216d
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