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FDA 510(k)

Lyric4 Hearing Aid

K-Number: K232999 · 2024-04-11

ApplicantSonova AG
Decision Date2024-04-11
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Lyric4 Hearing Aid is a medical device manufactured by Sonova AG. It received FDA 510(k) clearance on 2024-04-11 under approval number K232999. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lyric4 Hearing Aid?

Lyric4 Hearing Aid is a medical device that received FDA 510(k) clearance on 2024-04-11. It is manufactured by Sonova AG. The 510(k) number is K232999.

When was Lyric4 Hearing Aid approved by the FDA?

Lyric4 Hearing Aid received FDA 510(k) clearance on 2024-04-11, under approval number K232999.

What company makes Lyric4 Hearing Aid?

Lyric4 Hearing Aid is manufactured by Sonova AG.

What is the FDA product code for Lyric4 Hearing Aid?

The FDA product code for Lyric4 Hearing Aid is ESD.

Related Clinical Trials

NCT07388784 Exploration of the Functional Effect of Modified Gain Precalculation on Soft Speech Intelligibility RECRUITING

Other Devices by Sonova AG

K230538All-Day Clear Slim ADCS1 Hearing Aid. All-Day Clear ADC1 Hearing Aid

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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