BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1
K-Number: K864823 · 1987-01-06
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Device Summary
Frequently Asked Questions
What is the BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1?
BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1 is a medical device that received FDA 510(k) clearance on 1987-01-06. The listed applicant is Bernafon, Inc.. The 510(k) number is K864823.
When did BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1 receive FDA 510(k) clearance?
BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1 received FDA 510(k) clearance on 1987-01-06, under 510(k) number K864823.
Who is the listed applicant for BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1?
The FDA 510(k) record lists Bernafon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1?
The FDA product code for BEHIND THE EAR HEARING AIDS, BERNAFON COLIBRI, C1 is ESD.
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 Bernafon, Inc. 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: ESD)
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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