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FDA 510(k), K173926, DORADOnova MR3T
FDA 510(k), K173926, DORADOnova MR3T
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510(K) Number: K173926
Device Name: DORADOnova MR3T
Manufacturer: Martin Pfabel
Device Classification Name: Accelerator, Linear, Medical
Regulation Number: IYE
Classification Product Code: 12/26/2017
Date Received: 09/14/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: DORADOnova MR3T
Manufacturer: Martin Pfabel
Device Classification Name: Accelerator, Linear, Medical
Regulation Number: IYE
Classification Product Code: 12/26/2017
Date Received: 09/14/2018
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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