FDA 510(k) Applications for Medical Device Product Code "JLB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K992140 | ABAXIS, INC. | PICCOLO METLYTE 7 REAGENT DISC | 08/26/1999 |
K971817 | OLYMPUS AMERICA, INC. | OLYMPUS CK-MB REAGENT | 06/11/1997 |