
Medix Biotech, Inc.
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MEDIX BIOTECH STREP A ANTIGEN DETECTION TEST (MODIFICATION) is an FDA 510(k)-cleared medical device (K952873) manufactured by Medix Biotech, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 7, 1995. Regulation: 8.

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