Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SonoBook Series Diagnostic Ultrasound System

K-Number: K170374 · 2017-06-06

Decision Date2017-06-06
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SonoBook Series Diagnostic Ultrasound System is a medical device manufactured by Chison Medical Imaging Co., Ltd.. It received FDA 510(k) clearance on 2017-06-06 under approval number K170374. 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 SonoBook Series Diagnostic Ultrasound System?

SonoBook Series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2017-06-06. It is manufactured by Chison Medical Imaging Co., Ltd.. The 510(k) number is K170374.

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

SonoBook Series Diagnostic Ultrasound System received FDA 510(k) clearance on 2017-06-06, under approval number K170374.

What company makes SonoBook Series Diagnostic Ultrasound System?

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

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

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

Related Clinical Trials

Related PubMed Literature

Other Devices by Chison Medical Imaging Co., Ltd.

Related Devices (Code: IYN)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.