Medisense, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medisense, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Medisense, Inc. has 15 FDA 510(k) cleared chemistry devices. Based in Cambridge, US.
Historical record: 15 cleared submissions from 1990 to 1999.
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 - Medisense, Inc.
15 devices
Cleared
Jul 09, 1999
PRECISION XTRA ADVANCED DIABETES MANAGEMENT SYSTEM, PRECISION BLOOD GLUCOSE...
Chemistry
276d
Cleared
Dec 08, 1998
PRECISION PCX POINT OF CARE MANAGEMENT SYSTEM , QC MANAGER DATA MANAGER...
Chemistry
160d
Cleared
Nov 20, 1998
PRECISION A1C HOME HBA1C SAMPLE COLLECTION KIT
Hematology
65d
Cleared
Aug 08, 1997
PRECISION QID BLOOD GLUCOSE TEST STRIP, PRECISION G BLOOD GLUCOSE TEST STRIP
Chemistry
84d
Cleared
Feb 20, 1997
PRECISION G BLOOD GLUCOSE TESTING SYSTEM
Chemistry
160d
Cleared
Jul 26, 1996
PRECISION QID BLOOD GLUCOSE TEST STRIP
Chemistry
71d
Cleared
Jun 21, 1996
EXACTECH RSG BLOOD GLUCOSE TESTING SYSTEM
Chemistry
74d
Cleared
Jun 14, 1995
PRECISION LINK BLOOD GLUCOSE DATA MANAGEMENT SYSTEM
Chemistry
64d
Cleared
Mar 23, 1995
QUICKPRO BLOOD GLUCOSE TESTING SYSTEM
Chemistry
206d
Cleared
Mar 23, 1995
PRECISION Q I D BLOOD GLUCOSE TEST STRIPS
Chemistry
112d
Cleared
Jul 10, 1990
MEDISENSE PEN 2/COMPANION 2 BLOOD GLUCOSE SYSTEM
Chemistry
95d
Cleared
Jun 12, 1990
SATELLITE C BLOOD CHOLESTEROL MONITORING SYSTEM
Chemistry
211d