FDA 510(k) Applications for Medical Device Product Code "LRH"
(Instrument For Auto Reader Of Overnight Microorganism Identification System)

FDA 510(k) Number Applicant Device Name Decision Date
K962609 BIOMERIEUX VITEK, INC. GRAM NEGATIVE IDENTIFICATION PLUS CARD 08/30/1996
K961042 DADE MICROSCAN, INC. MICROSCAN RAPID GRAM-NEGATIVE INDENTIFICATION TYPE 3 PANEL 05/30/1996


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