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FDA 510(k), K173739, ALOKA ARIETTA 850
FDA 510(k), K173739, ALOKA ARIETTA 850
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510(K) Number: K173739
Device Name: ALOKA ARIETTA 850
Manufacturer: Hitachi Healthcare Americas Corporation
Device Classification Name: System, Imaging, Pulsed Doppler, Ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 12/07/2017
Decision Date: 02/28/2018
Regulation Medical Specialty: Radiology
Device Name: ALOKA ARIETTA 850
Manufacturer: Hitachi Healthcare Americas Corporation
Device Classification Name: System, Imaging, Pulsed Doppler, Ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 12/07/2017
Decision Date: 02/28/2018
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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