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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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