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Peter M. Rothenberg, M.D.
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TEMPORARY TRANSVENOUS PACEMAKER PLACEMENT ASSIST DEVICE is an FDA 510(k)-cleared medical device (K032613) manufactured by Peter M. Rothenberg, M.D.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 19, 2003. Regulation: 8.