
Cryomedical Sciences, Inc.
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ACCUPROBE 450, ACCUPROBE 550/530 AND THE ACCUPROBE 600 SERIES is an FDA 510(k)-cleared medical device (K973190) manufactured by Cryomedical Sciences, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 1997. Regulation: 8.