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FDA 510(k), K150861, QBit Series Diagnostic Ultrasound System
FDA 510(k), K150861, QBit Series Diagnostic Ultrasound System
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510(K) Number: K150861
Device Name: QBit Series Diagnostic Ultrasound System
Manufacturer: CHISON MEDICAL IMAGING CO., LTD.
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 04/01/2015
Decision Date: 07/28/2015
Regulation Medical Specialty: Radiology
Device Name: QBit Series Diagnostic Ultrasound System
Manufacturer: CHISON MEDICAL IMAGING CO., LTD.
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 04/01/2015
Decision Date: 07/28/2015
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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