Medical Device Manufacturer · US , Mchenry , IL

Skytron, Div. the Kmw Group, Inc. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1981

Recent clearances: AURORA LED SERIES SURGICAL LIGHTS, STELLAR SERIES SURGICAL LIGHTS WITH HERMES, STELLAR

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.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Skytron, Div. the Kmw Group, Inc. is one of 13825 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Skytron, Div. the Kmw Group, Inc.

19 devices

1-12 of 19

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

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