FDA 510(k) Applications for Medical Device Product Code "DID"
(Bacillus Subtlis Microbiology Assay, Tobramycin)

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


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