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FDA 510(k)

MODEL 341H (HEARING AID)

K-Number: K792464 · 1980-01-09

Decision Date1980-01-09
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL 341H (HEARING AID) is the device name listed in this FDA 510(k) record. The listed applicant is Telex Communications, Inc.. It received FDA 510(k) clearance on 1980-01-09 under 510(k) number K792464. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 341H (HEARING AID)?

MODEL 341H (HEARING AID) is a medical device that received FDA 510(k) clearance on 1980-01-09. The listed applicant is Telex Communications, Inc.. The 510(k) number is K792464.

When did MODEL 341H (HEARING AID) receive FDA 510(k) clearance?

MODEL 341H (HEARING AID) received FDA 510(k) clearance on 1980-01-09, under 510(k) number K792464.

Who is the listed applicant for MODEL 341H (HEARING AID)?

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 341H (HEARING AID)?

The FDA product code for MODEL 341H (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 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.

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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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