PARI PEP THERAPY SYSTEM

PARI PEP THERAPY SYSTEM is an FDA 510(k)-cleared medical device (K972042) manufactured by Pari Holding Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 1997. Regulation: 8.