FDA 510(k) Applications Submitted by Ken Revennaugh

FDA 510(k) Number Submission Date Device Name Applicant
K162001 07/20/2016 1.5T and 3.0T 16 CH GE Shoulder Coils INVIVO CORPORATION
K162177 08/04/2016 dS FootAnkle I6CH 1.5T Coil Invivo Corporation
K162863 10/13/2016 dS Small Extremity 16CH 1.5T Coil INVIVO THERAPEUTICS CORPORATION
K153073 10/22/2015 UroNav (Version 2.0) INVIVO CORPORATION
K182561 09/18/2018 UroNav (Version 3.0) Invivo Corporation


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