FDA 510(k) Applications Submitted by Dornoch Medical Systems

FDA 510(k) Number Submission Date Device Name Applicant
K190789 03/27/2019 IntelliCartTM System Dornoch Medical Systems
K172481 08/16/2017 IntelliCart System Dornoch Medical Systems
K162421 08/30/2016 IntelliCartTM System DORNOCH MEDICAL SYSTEMS


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