FDA 510(k) Applications for Medical Device Product Code "CHG"
(Acid, Phosphoric-Tungstic (Spectrophotometric), Chloride)

FDA 510(k) Number Applicant Device Name Decision Date
K934588 DIAGNOSTIC CHEMICALS LTD. CHLORIDE (MF) ASSAY 02/18/1994
K941807 INTERSECT SYSTEMS, INC. INTERSECT SYSTEMS' NON-MERCURIC CHLORIDE REAGENT 09/14/1994
K903103 SYNERMED, INC. SYNERMED CHLORIDE REAGENT KIT 08/09/1990


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