
Diagnostic Hybrids, Inc.
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D3 DFA METAPNEUMOVIRUS IDENTIFICATION KIT is an FDA 510(k)-cleared medical device (K090073) manufactured by Diagnostic Hybrids, 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 March 5, 2009. Regulation: 8.