FDA 510(k)

ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System

K-Number: K173957 · 2018-02-01

ApplicantSiemens Medical Solutions USA, Inc.

Decision Date2018-02-01

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2018-02-01 under approval number K173957. 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 ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System?

ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2018-02-01. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K173957.

When was ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System approved by the FDA?

ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System received FDA 510(k) clearance on 2018-02-01, under approval number K173957.

What company makes ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System?

ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System?

The FDA product code for ACUSON NX3 Diagnostic Ultrasound System; ACUSON NX3 ELITE Diagnostic Ultrasound System is IYN.

Related Clinical Trials

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Related PubMed Literature

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Related Devices (Code: IYN)

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Official Source

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