FDA 510(k) Applications for Medical Device Product Code: GKG (Centrifuge, Hematocrit)

FDA 510(k) Applications for Medical Device Product Code "GKG"
(Centrifuge, Hematocrit)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K961803	MICRO DIAGNOSTICS CORP.	SPUNCRIT (MODEL DRC-40)	07/05/1996
K955795	NOVONX, INC.	MULTI-CENTRIFUGE	03/29/1996

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