
Kindel & Anderson
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RIONET HEARING AID is an FDA 510(k)-cleared medical device (K802812) manufactured by Kindel & Anderson. 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 November 25, 1980. Regulation: 8.

Ansell
SKU MSC846624

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SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031