
Cryomedical Sciences, Inc.
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ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880 is an FDA 510(k)-cleared medical device (K982055) 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 September 7, 1998. Regulation: 8.