Sheathing Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sheathing Technologies, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Sheathing Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Morgan Hill, US.
Historical record: 7 cleared submissions from 1999 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sheathing Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sheathing Technologies, Inc.
7 devices
Cleared
Mar 04, 2016
Sheathes Ultrasound Probe Covers
Radiology
120d
Cleared
Feb 06, 2013
SHEATHES STERILE ULTRASOUND GEL
Radiology
29d
Cleared
Jun 22, 2012
SHEATHES ULTRASOND GEL
Radiology
268d
Cleared
Aug 03, 2010
COLONOSCOPE/SIGMOIDOSCOPE SHEATHES
Gastroenterology & Urology
117d
Cleared
Sep 28, 2009
SHEATHESISO ULTRASOUND TRANSDUCER COVER
Radiology
101d
Cleared
Feb 28, 2005
SHEATHES NEEDLE GUIDE, MODEL NG-SR-A-484-KIT (THERE WILL BE VARIOUS MODEL...
Radiology
77d
Cleared
Apr 21, 1999
SHEATHES (NON-LATEX), STERILE
Radiology
92d