
Microphage, Inc.
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KEYPATH MRSA/MSSA BLOOD CULTURE TEST-BT is an FDA 510(k)-cleared medical device (K120563) manufactured by Microphage, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 29, 2012. Regulation: 8.

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