
Pari Respiratory Equipment, Inc.
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PARI PEP S is an FDA 510(k)-cleared medical device (K090829) manufactured by Pari Respiratory Equipment, 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 July 20, 2009. Regulation: 8.

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