
Physio-Control Corp.
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ADR-10600(ADR 400),10601 (ADR 300) is an FDA 510(k)-cleared medical device (K791342) manufactured by Physio-Control Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 15, 1979. Regulation: 8.