
Chattanooga Group, Inc.
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PRESSSION, SEQUENTIAL is an FDA 510(k)-cleared medical device (K921608) manufactured by Chattanooga Group, 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 December 29, 1992. Regulation: 8.

ADC
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3M Littmann
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Welch Allyn
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