Eko Devices, Inc.
Eko Analysis Software
SKU K192004UPC MWI
In Stock
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IIFDA 510(k) Cleared (K192004)
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Free shipping on orders over $99 · 30-day returns
Eko Devices, Inc.
Free shipping on orders over $99 · 30-day returns
Eko Analysis Software is an FDA 510(k)-cleared medical device (K192004) manufactured by Eko Devices, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 14, 2020. Regulation: 8.
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