COCHLEAR BAHA 4 SOUND PROCESSOR
K-Number: K132278 · 2013-09-26
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Device Summary
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.
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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