POST-AURICULAR HEARING AID HC 880
K-Number: K771356 · 1977-07-29
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Device Summary
Frequently Asked Questions
What is the POST-AURICULAR HEARING AID HC 880?
POST-AURICULAR HEARING AID HC 880 is a medical device that received FDA 510(k) clearance on 1977-07-29. The listed applicant is Hc Electronics. The 510(k) number is K771356.
When did POST-AURICULAR HEARING AID HC 880 receive FDA 510(k) clearance?
POST-AURICULAR HEARING AID HC 880 received FDA 510(k) clearance on 1977-07-29, under 510(k) number K771356.
Who is the listed applicant for POST-AURICULAR HEARING AID HC 880?
The FDA 510(k) record lists Hc Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POST-AURICULAR HEARING AID HC 880?
The FDA product code for POST-AURICULAR HEARING AID HC 880 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 Hc Electronics 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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