Pluromed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pluromed, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Pluromed, Inc. has 4 FDA 510(k) cleared medical devices. Based in Woburn, US.
Historical record: 4 cleared submissions from 2009 to 2011. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pluromed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pluromed, Inc.
4 devices
Cleared
Mar 16, 2011
BACKSTOP CATHETER
Gastroenterology & Urology
22d
Cleared
Jan 07, 2011
BACKSTOP CATHETER
Gastroenterology & Urology
52d
Cleared
Jun 02, 2009
BACKSTOP AND BACKSTOP INJECTOR
Gastroenterology & Urology
103d
Cleared
May 15, 2009
BACKSTOP CATHETER, MODEL 60-0000-3100
Gastroenterology & Urology
100d