Diatech, Inc.
FIBRINOGEN TEST
SKU K834571UPC KQJ
In Stock
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IIFDA 510(k) Cleared (K834571)
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Free shipping on orders over $99 · 30-day returns
Diatech, Inc.
Free shipping on orders over $99 · 30-day returns
FIBRINOGEN TEST is an FDA 510(k)-cleared medical device (K834571) manufactured by Diatech, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 3, 1984. Regulation: 8.
