
Promex, Inc.
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PROMEX ENT TISSUE REMOVAL SYSTEM is an FDA 510(k)-cleared medical device (K972865) manufactured by Promex, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 28, 1997. Regulation: 8.

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