MODEL 800, BEHIND-THE-EAR HEARING AID
K-Number: K911706 · 1991-05-17
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Device Summary
Frequently Asked Questions
What is the MODEL 800, BEHIND-THE-EAR HEARING AID?
MODEL 800, BEHIND-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1991-05-17. The listed applicant is Electone, Inc.. The 510(k) number is K911706.
When did MODEL 800, BEHIND-THE-EAR HEARING AID receive FDA 510(k) clearance?
MODEL 800, BEHIND-THE-EAR HEARING AID received FDA 510(k) clearance on 1991-05-17, under 510(k) number K911706.
Who is the listed applicant for MODEL 800, BEHIND-THE-EAR 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 MODEL 800, BEHIND-THE-EAR HEARING AID?
The FDA product code for MODEL 800, BEHIND-THE-EAR 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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