MODEL 342 HEARING AIDS
K-Number: K790354 · 1979-03-06
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Device Summary
Frequently Asked Questions
What is the MODEL 342 HEARING AIDS?
MODEL 342 HEARING AIDS is a medical device that received FDA 510(k) clearance on 1979-03-06. The listed applicant is Telex Communications, Inc.. The 510(k) number is K790354.
When did MODEL 342 HEARING AIDS receive FDA 510(k) clearance?
MODEL 342 HEARING AIDS received FDA 510(k) clearance on 1979-03-06, under 510(k) number K790354.
Who is the listed applicant for MODEL 342 HEARING AIDS?
The FDA 510(k) record lists Telex Communications, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 342 HEARING AIDS?
The FDA product code for MODEL 342 HEARING AIDS 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 Telex Communications, 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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