NELLCOR PURITAN BENNETT GEMINI

NELLCOR PURITAN BENNETT GEMINI is an FDA 510(k)-cleared medical device (K972248) manufactured by Nellcor Puritan Bennett, 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 September 11, 1997. Regulation: 8.