FDA 510(k) Applications Submitted by CHRONIMED, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K010039 01/05/2001 QUICKTEK BLOOD GLUCOSE SYSTEM, QUICKTEK BLOOD GLUCOSE METER, QUICKTEK BLOOD GLUCOSE STRIPS, QUICKTEK CONTROL SOLUTION CHRONIMED, INC.
K980573 02/17/1998 SENSOREX BLOOD GLUCOSE MONITORING SYSTEM CHRONIMED, INC.
K963544 09/04/1996 SUPREME II METER CHRONIMED, INC.
K983432 09/29/1998 SUPREME II CONTROL SOLUTIONS CHRONIMED, INC.
K981555 05/01/1998 DIASCREEN REAGENT STRIPS CHRONIMED, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact