Prognostix, Inc.
CARDIOMPO TEST
SKU K050029UPC NTV
In Stock
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IIFDA 510(k) Cleared (K050029)
1
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Prognostix, Inc.
Free shipping on orders over $99 · 30-day returns
CARDIOMPO TEST is an FDA 510(k)-cleared medical device (K050029) manufactured by Prognostix, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 9, 2005. Regulation: 8.
