
Burdick, Inc.
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ALTAIR 6100 CASSETTE RECORDER is an FDA 510(k)-cleared medical device (K942438) manufactured by Burdick, 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 August 4, 1994. Regulation: 8.

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