HEARING AID, POST-AURICULAR
K-Number: K782053 · 1978-12-15
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Device Summary
Frequently Asked Questions
What is the HEARING AID, POST-AURICULAR?
HEARING AID, POST-AURICULAR is a medical device that received FDA 510(k) clearance on 1978-12-15. The listed applicant is Hc Electronics. The 510(k) number is K782053.
When did HEARING AID, POST-AURICULAR receive FDA 510(k) clearance?
HEARING AID, POST-AURICULAR received FDA 510(k) clearance on 1978-12-15, under 510(k) number K782053.
Who is the listed applicant for HEARING AID, POST-AURICULAR?
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 HEARING AID, POST-AURICULAR?
The FDA product code for HEARING AID, POST-AURICULAR 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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