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Rhino Metrics A/S
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RHINOSCAN MODEL SRE2000/ SRE2100 WITH ACOUSTIC RHINOMETRY MODULE is an FDA 510(k)-cleared medical device (K000406) manufactured by Rhino Metrics A/S. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 16, 2000. Regulation: 8.