FDA 510(k) Applications Submitted by MEDISENSE, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K961337 |
04/08/1996 |
EXACTECH RSG BLOOD GLUCOSE TESTING SYSTEM |
MEDISENSE, INC. |
| K983253 |
09/16/1998 |
PRECISION A1C HOME HBA1C SAMPLE COLLECTION KIT |
MEDISENSE, INC. |
| K962295 |
05/16/1996 |
PRECISION QID BLOOD GLUCOSE TEST STRIP |
MEDISENSE, INC. |
| K971812 |
05/16/1997 |
PRECISION QID BLOOD GLUCOSE TEST STRIP, PRECISION G BLOOD GLUCOSE TEST STRIP |
MEDISENSE, INC. |
| K982303 |
07/01/1998 |
PRECISION PCX POINT OF CARE MANAGEMENT SYSTEM , QC MANAGER DATA MANAGER SYSTEM, PRECISION G PLUS BLOOD GLUCOSE TEST ST |
MEDISENSE, INC. |
| K963676 |
09/13/1996 |
PRECISION G BLOOD GLUCOSE TESTING SYSTEM |
MEDISENSE, INC. |
| K983504 |
10/06/1998 |
PRECISION XTRA ADVANCED DIABETES MANAGEMENT SYSTEM, PRECISION BLOOD GLUCOSE TEST STRIPS, PRECISION XTRA B-KETONE TEST ST |
MEDISENSE, INC. |
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