Scottcare Corporation
GENESIS ECP
SKU K081359UPC DRN
In Stock
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IIFDA 510(k) Cleared (K081359)
1
Free shipping on orders over $99 · 30-day returns
Scottcare Corporation
Free shipping on orders over $99 · 30-day returns
GENESIS ECP is an FDA 510(k)-cleared medical device (K081359) manufactured by Scottcare Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 28, 2008. Regulation: 8.
