
Medical Devices/Padpro, Inc.
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DEFIBRILLATOR CABLE TESTER, MODEL DT2200 is an FDA 510(k)-cleared medical device (K061606) manufactured by Medical Devices/Padpro, 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 June 20, 2006. Regulation: 8.