
Rusch, Inc.
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RUSCH AGT PVC PREFORM NASAL TRACH TUB/CUF W/MUR EY is an FDA 510(k)-cleared medical device (K931164) manufactured by Rusch, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 1993. Regulation: 8.

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