THE ANSWER HEARING AID
K-Number: K854438 · 1986-02-24
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Device Summary
Frequently Asked Questions
What is the THE ANSWER HEARING AID?
THE ANSWER HEARING AID is a medical device that received FDA 510(k) clearance on 1986-02-24. The listed applicant is Electone, Inc.. The 510(k) number is K854438.
When did THE ANSWER HEARING AID receive FDA 510(k) clearance?
THE ANSWER HEARING AID received FDA 510(k) clearance on 1986-02-24, under 510(k) number K854438.
Who is the listed applicant for THE ANSWER HEARING AID?
The FDA 510(k) record lists Electone, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE ANSWER HEARING AID?
The FDA product code for THE ANSWER HEARING AID 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 Electone, 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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