EYEGLASS HEARING AID
K-Number: K760609 · 1976-09-21
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Device Summary
Frequently Asked Questions
What is the EYEGLASS HEARING AID?
EYEGLASS HEARING AID is a medical device that received FDA 510(k) clearance on 1976-09-21. The listed applicant is Zenith Hearing Instrument Co.. The 510(k) number is K760609.
When did EYEGLASS HEARING AID receive FDA 510(k) clearance?
EYEGLASS HEARING AID received FDA 510(k) clearance on 1976-09-21, under 510(k) number K760609.
Who is the listed applicant for EYEGLASS HEARING AID?
The FDA 510(k) record lists Zenith Hearing Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EYEGLASS HEARING AID?
The FDA product code for EYEGLASS 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.
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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