
Cederroth, Inc. USA
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RESUSCITATION MASK is an FDA 510(k)-cleared medical device (K820059) manufactured by Cederroth, Inc. USA. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 25, 1982. Regulation: 8.

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