Name: DIRECTIGEN COMBO MENINGITIS TEST
Brand: Bd Becton Dickinson Vacutainer Systems Preanalytic
SKU: K860768

DIRECTIGEN COMBO MENINGITIS TEST is an FDA 510(k)-cleared medical device (K860768) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 12, 1986. Regulation: 8.

DIRECTIGEN COMBO MENINGITIS TEST

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