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FDA 510(k)

COCHLEAR BAHA 4 SOUND PROCESSOR

K-Number: K132278 · 2013-09-26

Decision Date2013-09-26
Product CodeLXB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

COCHLEAR BAHA 4 SOUND PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Cochlear Americas. It received FDA 510(k) clearance on 2013-09-26 under 510(k) number K132278. The device is classified under product code LXB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COCHLEAR BAHA 4 SOUND PROCESSOR?

COCHLEAR BAHA 4 SOUND PROCESSOR is a medical device that received FDA 510(k) clearance on 2013-09-26. The listed applicant is Cochlear Americas. The 510(k) number is K132278.

When did COCHLEAR BAHA 4 SOUND PROCESSOR receive FDA 510(k) clearance?

COCHLEAR BAHA 4 SOUND PROCESSOR received FDA 510(k) clearance on 2013-09-26, under 510(k) number K132278.

Who is the listed applicant for COCHLEAR BAHA 4 SOUND PROCESSOR?

The FDA 510(k) record lists Cochlear Americas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COCHLEAR BAHA 4 SOUND PROCESSOR?

The FDA product code for COCHLEAR BAHA 4 SOUND PROCESSOR is LXB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Cochlear Americas as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 18 devices →

Related Devices (Code: LXB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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