Earlitec Diagnostics, Inc.
EarliPoint System
SKU K213882UPC QPF
In Stock
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IIFDA 510(k) Cleared (K213882)
1
Free shipping on orders over $99 · 30-day returns
Earlitec Diagnostics, Inc.
Free shipping on orders over $99 · 30-day returns
EarliPoint System is an FDA 510(k)-cleared medical device (K213882) manufactured by Earlitec Diagnostics, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 7, 2022. Regulation: 8.
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