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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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