FDA 510(k) Applications Submitted by DALE DEMBROW

FDA 510(k) Number Submission Date Device Name Applicant
K951799 04/19/1995 VARICELLA-ZOSTER VIRUS DIRECT IMMUNOFLUORESCENCE ASSAY LIGHT DIAGNOSTICS
K951821 04/20/1995 CYTOMEGALOVIRUS DIRECT IMMUNOFLUORESCENCE ASSAY LIGHT DIAGNOSTICS


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