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FDA 510(k)

3D Echo

K-Number: K172513 · 2017-09-14

ApplicantJointvue, LLC
Decision Date2017-09-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3D Echo is a medical device manufactured by Jointvue, LLC. It received FDA 510(k) clearance on 2017-09-14 under approval number K172513. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3D Echo?

3D Echo is a medical device that received FDA 510(k) clearance on 2017-09-14. It is manufactured by Jointvue, LLC. The 510(k) number is K172513.

When was 3D Echo approved by the FDA?

3D Echo received FDA 510(k) clearance on 2017-09-14, under approval number K172513.

What company makes 3D Echo?

3D Echo is manufactured by Jointvue, LLC.

What is the FDA product code for 3D Echo?

The FDA product code for 3D Echo is LLZ.

Other Devices by Jointvue, LLC

K173329jFit Surgical Planner K2116563D Echo v1.1

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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.

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