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Acclarent, Inc.
Free shipping on orders over $99 · 30-day returns
RELIEVA SEEKER BALLOON SINUPLASTY SYSTEM is an FDA 510(k)-cleared medical device (K120280) manufactured by Acclarent, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 4, 2012. Regulation: 8.

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