EAGLE I HEARING AID
K-Number: K811988 · 1981-07-28
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Device Summary
Frequently Asked Questions
What is the EAGLE I HEARING AID?
EAGLE I HEARING AID is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Electone, Inc.. The 510(k) number is K811988.
When did EAGLE I HEARING AID receive FDA 510(k) clearance?
EAGLE I HEARING AID received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811988.
Who is the listed applicant for EAGLE I 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 EAGLE I HEARING AID?
The FDA product code for EAGLE I 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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