FDA 510(k) Applications for Medical Device Product Code "MXB"
(Test,Vaginal,Bacterial Sialidase)

FDA 510(k) Number Applicant Device Name Decision Date
K993732 GRYPHUS DIAGNOSTICS, L.L.C. BVBLUE 05/15/2000
K050755 GRYPHUS DIAGNOSTICS, LLC MODIFICATION TO BVBLUE 04/06/2005


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