Clinical Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clinical Innovations, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Clinical Innovations, Inc. has 9 FDA 510(k) cleared medical devices. Based in Murray, US.
Historical record: 9 cleared submissions from 1994 to 2003. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Clinical Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Clinical Innovations, Inc.
9 devices
Cleared
Sep 17, 2003
FETAL SPIRAL ELECTRODE, MODEL FSE07000
Obstetrics & Gynecology
196d
Cleared
Jan 07, 2003
COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL...
Gastroenterology & Urology
201d
Cleared
May 03, 2001
SOFT BEAT FETAL HEART RATE ELECTRODE MODEL SBT-7000
Obstetrics & Gynecology
177d
Cleared
Sep 22, 1998
KIWI SOFT CUP WITH PALM PUMP MODEL NUMBER VFE-6000S, KIWI MUSHROOM CUP WITH...
Obstetrics & Gynecology
169d
Cleared
Mar 02, 1998
COLPO CUP CVC-2000
Obstetrics & Gynecology
87d
Cleared
Feb 19, 1998
KOALA INTRAUTERINE PRESSURE CATHETER, KOALA EXTERNAL INTRAUTERINE PRESSURE...
Obstetrics & Gynecology
90d
Cleared
Nov 24, 1997
PRE-FILLED SYRINGE FOR KOALA IUP
Obstetrics & Gynecology
54d
Cleared
Apr 17, 1996
STORC INTRAUTERINE PRESSURE CATHETER
Obstetrics & Gynecology
173d
Cleared
Jul 26, 1994
CLEARVIEW UTERINE MANIPULATOR
Obstetrics & Gynecology
166d