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Neurovision Medical Products, Inc.
Free shipping on orders over $99 · 30-day returns
DRYTOUCH SUCTION STIMULATOR PROBE is an FDA 510(k)-cleared medical device (K110712) manufactured by Neurovision Medical Products, 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 June 27, 2011. Regulation: 8.

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