FDA 510(k) Applications for Medical Device Product Code: LOO (Reagent, Leishmanii Serological)

FDA 510(k) Applications for Medical Device Product Code "LOO"
(Reagent, Leishmanii Serological)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K023483	INBIOS INTL., INC.	KALAZAR DETECT	05/06/2003

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