
Cryocor, Inc.
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CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 is an FDA 510(k)-cleared medical device (K041890) manufactured by Cryocor, 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 21, 2004. Regulation: 8.