
G. Dundas Co.
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MODEL 5460 + 5480 POP-OFF VALVES is an FDA 510(k)-cleared medical device (K802591) manufactured by G. Dundas 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 November 11, 1980. Regulation: 8.

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