Inverness Medical Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inverness Medical Innovations, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Inverness Medical Innovations, Inc. has 6 FDA 510(k) cleared medical devices. Based in Waltham, US.
Historical record: 6 cleared submissions from 2001 to 2007. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Inverness Medical Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inverness Medical Innovations, Inc.
6 devices
Cleared
Nov 30, 2007
SMARTCHECK INR SYSTEM
Hematology
207d
Cleared
Jul 30, 2007
ISCHEMIA ALBUMIN COBALT BINDING TEST (ACB TEST) ASSAY
Chemistry
49d
Cleared
Feb 16, 2006
ISCHEMIA ALBUMIN COBALT BINDING TEST (ACB) ASSAY VERIFICATION SET
Chemistry
29d
Cleared
Dec 16, 2005
ISCHEMIA ALBUMIN COBALT BINDING TEST (ACB TEST)
Chemistry
30d
Cleared
Nov 30, 2001
ONE TOUCH FASTTAKE COMPACT BLOOD GLUCOSE MONITORING SYSTEM, ONE TOUCH ULTRA...
Chemistry
200d
Cleared
Jun 21, 2001
INDUO BLOOD GLUCOSE METER
Chemistry
27d