
Minntech Corp.
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MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM is an FDA 510(k)-cleared medical device (K092387) manufactured by Minntech Corp.. 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 April 4, 2010. Regulation: 8.

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