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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: KXA
Date Received: 06/14/2018
Decision Date: 07/10/2018
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: Workflow Box
Manufacturer: Gwilym Owen
Device Classification Name: Radiological Image Processing Software For Radiation Therapy
Regulation Number: QKB
Classification Product Code: KXA
Date Received: 06/14/2018
Decision Date: 07/10/2018
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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