FDA 510(k), K181572, Workflow Box

FDA 510(k), K181572, Workflow Box

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510(K) Number: K181572
Device Name: Workflow Box
Manufacturer: Gwilym Owen
Device Classification Name: Radiological Image Processing Software For Radiation Therapy
Regulation Number: QKB
Classification Product Code: 06/14/2018
Date Received: 07/10/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology

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