Promedic, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Promedic, Inc. - FDA 510(k) Cleared Devices
16
Total
14
Cleared
0
Denied
Promedic, Inc. has 14 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Historical record: 14 cleared submissions from 1995 to 2014.
Browse the FDA 510(k) cleared devices submitted by Promedic, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Promedic, Inc.
16 devices
Cleared
Apr 23, 2014
EUM 100PRO
Obstetrics & Gynecology
302d
Cleared
Jun 29, 2012
CLEARPATH 24
Gastroenterology & Urology
323d
Cleared
Dec 19, 2007
NON-IV ADAPTER FOR INFANT NG TUBE
Gastroenterology & Urology
83d
Cleared
Jul 11, 2006
BABYAIR
Anesthesiology
137d
Cleared
Jun 21, 2006
REVJET TURBO
Anesthesiology
85d
Cleared
Nov 09, 2005
PEDIATRIC FEEDING TUBE
Gastroenterology & Urology
26d
Cleared
Jun 17, 2003
URINARY CATHETERS
Gastroenterology & Urology
43d
Cleared
Mar 17, 2003
FENESTRATED INFUSION CATHETER
General Hospital
88d
Cleared
Jan 28, 2003
GAS SAMPLING LINES
Anesthesiology
96d
Cleared
Jul 16, 2002
INFANT FEEDING TUBES
Gastroenterology & Urology
195d
Cleared
Jun 24, 1997
FILTER
General Hospital
162d
Cleared
Jun 16, 1997
DATEX ENGSTOM MANUAL RESUSCITATOR
Anesthesiology
89d