FDA 510(k) Applications Submitted by Debbie Kidder

FDA 510(k) Number Submission Date Device Name Applicant
K070311 02/01/2007 CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261 MEDTRONIC VASCULAR
K170524 02/22/2017 Access AMH Beckman Coulter, Inc.
K082475 08/28/2008 REVEAL XT INSERTABLE CARDIAC MONITOR, MODEL 9529, REVEL DX INSERTABLE CARDIAC MONITOR, MODEL 9528 MEDTRONIC INC.


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