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FDA 510(k) Applications for Medical Device Product Code "DID"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K802038 | BECKMAN INSTRUMENTS, INC. | PHENYTOIN REAGENT TEST KIT | 10/23/1980 |
K780950 | MONITOR SCIENCE CORP. | BIO-MONITOR TOBRAMYCIN | 08/14/1978 |
K780182 | NEW ENGLAND NUCLEAR | TOBRAMYCIN 125I RIA KIT | 02/13/1978 |
K780048 | NICHOLS INSTITUTE DIAGNOSTICS | AMINOGLYCOSIDE TEST SYSTEM | 01/20/1978 |
K820773 | SYVA CO. | EMIT-ST URINE COCAINE METABOLITE ASSAY | 04/08/1982 |