
Precision Dynamics Corp.
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AGAR REDUCTION IN FORMULA FOR PDC 110 & 310 MEDIA is an FDA 510(k)-cleared medical device (K863164) manufactured by Precision Dynamics Corp.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 26, 1986. Regulation: 8.

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