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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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