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FDA 510(k) Applications for Medical Device Product Code "LRH"
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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 |