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FDA 510(k), K171594, Accuro
FDA 510(k), K171594, Accuro
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$149.00 USD
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510(K) Number: K171594
Device Name: Accuro
Manufacturer: Rivanna Medical, LLC
Device Classification Name: System, Imaging, Pulsed Echo, Ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 05/31/2017
Decision Date: 10/20/2017
Regulation Medical Specialty: Radiology
Device Name: Accuro
Manufacturer: Rivanna Medical, LLC
Device Classification Name: System, Imaging, Pulsed Echo, Ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 05/31/2017
Decision Date: 10/20/2017
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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