Name: ORTHO* CYTOMEGALOVIRUS IDENTIFICATION REAGENT
Brand: Ortho Diagnostic Systems, Inc.
SKU: K881932

ORTHO* CYTOMEGALOVIRUS IDENTIFICATION REAGENT is an FDA 510(k)-cleared medical device (K881932) manufactured by Ortho Diagnostic Systems, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 31, 1988. Regulation: 8.

ORTHO* CYTOMEGALOVIRUS IDENTIFICATION REAGENT

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