
Zymetx, Inc.
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VIRAZYME INFLUENZA ID TEST FOR INFLUENZA TYPES A AND B VIRUSES is an FDA 510(k)-cleared medical device (K971494) manufactured by Zymetx, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 9, 1997. Regulation: 8.

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