
Pmt Corp.
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PMT SPHENOIDAL ELECTRODE AND ACCESSORY, MODEL 2101-31 AND 2102-31 SERIES is an FDA 510(k)-cleared medical device (K033730) manufactured by Pmt Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 2, 2004. Regulation: 8.

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