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FDA 510(k)

EBit Series Diagnostic Ultrasound System

K-Number: K162172 · 2016-09-14

Decision Date2016-09-14
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EBit Series Diagnostic Ultrasound System is a medical device manufactured by Chison Medical Imaging Co., Ltd.. It received FDA 510(k) clearance on 2016-09-14 under approval number K162172. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBit Series Diagnostic Ultrasound System?

EBit Series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2016-09-14. It is manufactured by Chison Medical Imaging Co., Ltd.. The 510(k) number is K162172.

When was EBit Series Diagnostic Ultrasound System approved by the FDA?

EBit Series Diagnostic Ultrasound System received FDA 510(k) clearance on 2016-09-14, under approval number K162172.

What company makes EBit Series Diagnostic Ultrasound System?

EBit Series Diagnostic Ultrasound System is manufactured by Chison Medical Imaging Co., Ltd..

What is the FDA product code for EBit Series Diagnostic Ultrasound System?

The FDA product code for EBit Series Diagnostic Ultrasound System is IYN.

Related Clinical Trials

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Official Source

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