
Hans Rudolph, Inc.
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HRI 6500, 6600 AND 6700 SERIES V2MASKS is an FDA 510(k)-cleared medical device (K071149) manufactured by Hans Rudolph, 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 January 31, 2008. Regulation: 8.