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

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