
Mecta Corp.
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SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M. is an FDA 510(k)-cleared medical device (K965070) manufactured by Mecta 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 March 5, 1997. Regulation: 8.

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