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FDA 510(k), K173090, Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4
FDA 510(k), K173090, Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4
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510(K) Number: K173090
Device Name: Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4
Manufacturer: Toshiba Medical Systems Corporation
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 09/29/2017
Decision Date: 01/11/2018
Regulation Medical Specialty: Radiology
Device Name: Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4
Manufacturer: Toshiba Medical Systems Corporation
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 09/29/2017
Decision Date: 01/11/2018
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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