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.
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
Cleared
Jul 15, 1996
BURLEW INFANT HOOD
Anesthesiology
39d
Cleared
Nov 09, 1995
BUONAFEDE PNEUMATIC SLEEVE
General & Plastic Surgery
64d
Cleared
Jun 14, 1995
PRESSURIZER
General Hospital
48d
Cleared
Jun 07, 1995
AIR-SOFT-DISPOSABLE, ANESTHESISA/RESPIRATORY FACE MASK
Anesthesiology
92d