Microtek Medical, Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Microtek Medical, Inc. has 24 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1984 to 2011. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Microtek Medical, Inc. Filter by specialty or product code using the sidebar.
24 devices
Cleared
May 05, 2011
VENODYNE V810
Cardiovascular
87d
Cleared
Feb 23, 2011
FREEDOMAIRE III SURGICAL HELMET SYSTEM MODEL 10322STK
General Hospital
140d
Cleared
Jan 25, 2007
MICROTEK MEDICAL SURGICAL GOWN/TOGA
General Hospital
120d
Cleared
May 31, 2006
MICROTEK MEDICAL WARMING DRAPE
General Hospital
125d
Cleared
May 17, 2005
MICROTEK EQUIPMENT DRAPES
General Hospital
97d
Cleared
Nov 27, 2002
CHILLBUSTER
Cardiovascular
85d
Cleared
May 16, 2002
VIVOSONIC DIANOSTIC ULTRASOUND IMAGING COUPLING MEDIA
Radiology
52d
Cleared
Oct 25, 2001
VENODYNE DVT ADVANTAGE PLUS
Cardiovascular
177d
Cleared
Jan 09, 2001
VENODYNE DVT ADVANTAGE MODEL 610
Cardiovascular
209d
Cleared
Jun 22, 1995
LESINSKI SURGICAL EAR DRESSING
General & Plastic Surgery
114d
Cleared
Nov 18, 1994
FLEXIBLE HYDROXYLAPATITE/SILICONE SOFT CHIN IMPLAN
General & Plastic Surgery
743d
Cleared
Nov 23, 1987
MICROTEK MINI-MAX DRILL SYSTEM
Dental
20d