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FDA 510(k) Applications for Medical Device Product Code "MXB"
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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 |