FDA 510(k) Applications for Medical Device Product Code "CEI"
(Uranyl Acetate/Zinc Acetate, Sodium)

FDA 510(k) Number Applicant Device Name Decision Date
K832552 MALLINCKRODT CRITICAL CARE SODIUM TEST KIT 09/20/1983
K043268 RANDOX LABORATORIES, LTD. SODIUM TEST KIT AND ELETROLYTE CAL 1 AND 2 02/15/2005
K914039 STERLING DIAGNOSTICS, INC. SODIUM REAGENT SET 10/31/1991
K902572 TECH INTL. CO. SODIUM REAGENT SET 07/10/1990


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