Medisense, Inc.
Medisense, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1999.
Top product codes for Medisense, Inc.
Recent clearances by Medisense, Inc.
- K983504 — PRECISION XTRA ADVANCED DIABETES MANAGEMENT SYSTEM, PRECISION BLOOD GLUCOSE TEST STRIPS, PRECISION XTRA B-KETONE TEST ST
- K982303 — PRECISION PCX POINT OF CARE MANAGEMENT SYSTEM , QC MANAGER DATA MANAGER SYSTEM, PRECISION G PLUS BLOOD GLUCOSE TEST ST
- K983253 — PRECISION A1C HOME HBA1C SAMPLE COLLECTION KIT
- K971812 — PRECISION QID BLOOD GLUCOSE TEST STRIP, PRECISION G BLOOD GLUCOSE TEST STRIP
- K963676 — PRECISION G BLOOD GLUCOSE TESTING SYSTEM
- K962295 — PRECISION QID BLOOD GLUCOSE TEST STRIP
- K961337 — EXACTECH RSG BLOOD GLUCOSE TESTING SYSTEM
- K952279 — PRECISION LINK BLOOD GLUCOSE DATA MANAGEMENT SYSTEM
- K944195 — QUICKPRO BLOOD GLUCOSE TESTING SYSTEM
- K945887 — PRECISION Q I D BLOOD GLUCOSE TEST STRIPS
- K901613 — MEDISENSE PEN 2/COMPANION 2 BLOOD GLUCOSE SYSTEM
- K896467 — SATELLITE C BLOOD CHOLESTEROL MONITORING SYSTEM
- K897118 — SATELLITE A BLOOD ACETAMINOPHEN MONITORING SYSTEM
- K897110 — SATELLITE K+ BLOOD POTASSIUM MONITORING SYSTEM
- K896951 — SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.