Prodesse, Inc.
MODIFICATION TO PROFLU+ ASSAY
SKU K081030UPC OCC
In Stock
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IIFDA 510(k) Cleared (K081030)
1
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Prodesse, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO PROFLU+ ASSAY is an FDA 510(k)-cleared medical device (K081030) manufactured by Prodesse, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 1, 2008. Regulation: 8.
