FDA 510(k) Applications Submitted by KATHI GUERRANT

FDA 510(k) Number Submission Date Device Name Applicant
K040641 03/10/2004 ULTRACINCH ABLATION DEVICE, ULTRACINCH ACCESSORY PACK, MODELS UC-8, UC-9, UC-10, UC-11, UC-12, UC-13, UC-14, UC-ACC-1 EPICOR MEDICAL, INC.
K022894 09/03/2002 EPICOR MEDICAL ABLATION SYSTEM EPICOR MEDICAL, INC.


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