FDA 510(k) Applications for Medical Device Product Code "DLB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K955448 | BEHRING DIAGNOSTICS, INC. | EMIT II LSD ASSAY, EMIT LSD CALIBRATORS & EMIT LSD CONTROLS | 02/23/1996 |
K955814 | MICROGENICS CORP. | CEDIA DAU LSD ASSAY | 02/09/1996 |
K961436 | ROCHE DIAGNOSTIC SYSTEMS, INC. | ABUSCREEN ONLINE LSD REAGENT (90 ML TEST KIT) | 06/21/1996 |