
Excell Company, LLC
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exCellerator Cervical Collection Device is an FDA 510(k)-cleared medical device (K182049) manufactured by Excell Company, LLC. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 24, 2019. Regulation: 8.

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