Lifescan, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lifescan, Inc. - FDA 510(k) Cleared Devices
42
Total
42
Cleared
0
Denied
Lifescan, Inc. has 42 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 42 cleared submissions from 1981 to 2013.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lifescan, Inc.
42 devices
Cleared
Dec 16, 2013
ONETOUCH REVEAL
General Hospital
117d
Cleared
Feb 07, 2013
ONETOUCH REVEAL DIABETES MANAGEMENT APPLICATION
Chemistry
349d
Cleared
Feb 11, 2011
ONE TOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
434d
Cleared
Dec 17, 2008
SYMPHONY METER REMOTE
General Hospital
100d
Cleared
Oct 22, 2008
ONETOUCH VITA BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
50d
Cleared
Jun 09, 2008
ONETOUCH ZOOM DIABETES MANAGEMENT PROGRAM
Chemistry
28d
Cleared
Apr 18, 2008
ONETOUCH ULTRALINK BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
155d
Cleared
Oct 05, 2007
ONETOUCH SELECT BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
25d
Cleared
Aug 16, 2006
MODIFICATION TO ONE TOUCH ULTRA BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
15d
Cleared
May 19, 2006
ONETOUCH ULTRAMINI BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
28d
Cleared
Jan 17, 2006
ONETOUCH ULTRA 2 BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
29d
Cleared
May 20, 2005
ONETOUCH ULTRA, INDUO AND ULTRASMART BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
183d
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