FDA 510(k) Applications Submitted by ROSANNE M SAVOL, R.A.C.

FDA 510(k) Number Submission Date Device Name Applicant
K960546 02/08/1996 CLINITEK 50 URINE CHEMISTRY ANALYZER BAYER CORP.
K960888 03/04/1996 CHEK-STIX U.T.I. SELF-TEST BAYER CORP.
K971276 04/07/1997 GLUCOMETER ENCORE QA+ BLOOD GLUCOSE METER BAYER CORP.
K982219 06/24/1998 MICROALBUSTIX REAGENT STRIPS BAYER CORP.
K972706 07/21/1997 CLINITEK MICROALBUMIN REAGENT STRIPS BAYER CORP.
K964630 11/19/1996 GLUCOMETER ELITE BLOOD GLUCOSE METER BAYER CORP.
K963142 08/13/1996 DCA 2000 + MICROALBUMIN/CREATININE ASSAY BAYER CORP.
K963500 09/03/1996 GLUCOMETER DEX DIABETES CARE SYSTEM BAYER CORP.
K964004 10/07/1996 GLUCOMETER ENCORE BLOOD GLUCOSE TEST STRIPS BAYER CORP.


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