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FDA 510(k), K182177, Accipiolx
FDA 510(k), K182177, Accipiolx
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510(K) Number: K182177
Device Name: Accipiolx
Manufacturer: Joshua Schulman
Device Classification Name: Radiological Computer-Assisted Triage And Notification Software
Regulation Number: QAS
Classification Product Code: 08/10/2018
Date Received: 10/26/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: Accipiolx
Manufacturer: Joshua Schulman
Device Classification Name: Radiological Computer-Assisted Triage And Notification Software
Regulation Number: QAS
Classification Product Code: 08/10/2018
Date Received: 10/26/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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