FDA 510(k) Applications Submitted by CRYOCOR, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K040552 03/02/2004 MODEL 3100 SERIES SHEATH INTRODUCER KITS, MODELS 3110, 3130 CRYOCOR, INC.
K041890 07/12/2004 CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12 CRYOCOR, INC.


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