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FDA 510(k)

TRV

K-Number: K192652 · 2020-05-27

ApplicantInteracoustics A/S
Decision Date2020-05-27
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

TRV is a medical device manufactured by Interacoustics A/S. It received FDA 510(k) clearance on 2020-05-27 under approval number K192652. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRV?

TRV is a medical device that received FDA 510(k) clearance on 2020-05-27. It is manufactured by Interacoustics A/S. The 510(k) number is K192652.

When was TRV approved by the FDA?

TRV received FDA 510(k) clearance on 2020-05-27, under approval number K192652.

What company makes TRV?

TRV is manufactured by Interacoustics A/S.

What is the FDA product code for TRV?

The FDA product code for TRV is LXV.

Other Devices by Interacoustics A/S

K163149VisualEyes K162037Eclipse with VEMP K173567Sera K191372Lyra K200529Orion K200534VisualEyes

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Related Devices (Code: LXV)

K173669K-D BalanceKing-Devick Technologies, Inc. K183661ClearEdge Balance SystemQuadrant Biosciences K190735EQ BalanceUpright Science, Inc. K200529OrionInteracoustics A/S K220231GyroStimUltrathera Technologies, Inc.

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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