
Respironics California, Inc.
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ESPRIT VENTILATOR WITH NICO-ESPRIT INTERFACE OPTION, MODEL V1000 is an FDA 510(k)-cleared medical device (K041412) manufactured by Respironics California, 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 17, 2004. Regulation: 8.