FDA 510(k) Applications for Medical Device Product Code "FJD"
(Detector, Leak, Blood)

FDA 510(k) Number Applicant Device Name Decision Date
K042322 HACH COMPANY STERICHEK BLOOD LEAK REAGENT STRIPS 12/07/2004
K123805 REPROCESSING PRODUCTS CORP. E-Z CHEK BLOOD LEAK TEST STRIPS 03/20/2013
K990206 SERIM RESEARCH CORP. SERIM BLOOD LEAK TEST STRIP 04/21/1999
K012115 SERIM RESEARCH CORP. SERIM BLOOD LEAK TEST STRIP-2 11/30/2001


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