
Amplifon S.P.A.
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AMPLAID A311 SERIES is an FDA 510(k)-cleared medical device (K983712) manufactured by Amplifon S.P.A.. 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 January 11, 1999. Regulation: 8.

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