Fidia Pharmaceutical Corp.
MODIFICATION OF BIONECT HYDROGEL FOAM
SKU K984267UPC MGQ
In Stock
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FDA 510(k) Cleared (K984267)
1
Free shipping on orders over $99 · 30-day returns
Fidia Pharmaceutical Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION OF BIONECT HYDROGEL FOAM is an FDA 510(k)-cleared medical device (K984267) manufactured by Fidia Pharmaceutical Corp.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on February 9, 1999.
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