
Welch Allyn, Inc.
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ATLAS MONITOR, MODELS 200,210,220 is an FDA 510(k)-cleared medical device (K022084) manufactured by Welch Allyn, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 25, 2002. Regulation: 8.