FDA 510(k) Applications Submitted by KARI CHRISTIANSON

FDA 510(k) Number Submission Date Device Name Applicant
K071309 05/09/2007 BLUE MAX BALLOON DILATATION CATHETER BOSTON SCIENTIFIC CORP.
K121878 06/28/2012 CARDIOBLATE CRYOFLEX SURGICAL ABLATION PROBES MEDTRONIC INC.
K182610 09/21/2018 Valleylab FT10 Electrosurgical Platform, Cardioblate BP2 Surgical Ablation Device, Cardioblate LP Surgical Ablation Device Medtronic
K123733 12/05/2012 CARDIOBLATE CRYOFLEX SURGICAL ABLATION SYSTEM MEDTRONIC INC.


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