
Applied BioCode, Inc.
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BioCode Respiratory Pathogen Panel (RPP) is an FDA 510(k)-cleared medical device (K192485) manufactured by Applied BioCode, 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 December 22, 2019. Regulation: 8.

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