
Diesse Diagnostica Senese S.P.A.
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COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USE is an FDA 510(k)-cleared medical device (K070062) manufactured by Diesse Diagnostica Senese S.P.A.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 29, 2007. Regulation: 8.