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Medafor, Inc.
Free shipping on orders over $99 · 30-day returns
Medafor Direct Gas-Assisted Application System is an FDA 510(k)-cleared medical device (K123325) manufactured by Medafor, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 23, 2013. Regulation: 8.

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