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FDA 510(k)

TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC

K-Number: K913494 · 1991-11-01

Decision Date1991-11-01
Product CodeEPF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC 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 1991-11-01 under 510(k) number K913494. The device is classified under product code EPF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC?

TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC is a medical device that received FDA 510(k) clearance on 1991-11-01. The listed applicant is Telex Communications, Inc.. The 510(k) number is K913494.

When did TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC receive FDA 510(k) clearance?

TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC received FDA 510(k) clearance on 1991-11-01, under 510(k) number K913494.

Who is the listed applicant for TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC?

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 TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC?

The FDA product code for TELEX TDR-4AA MONAURAL HEAR AID/WIRELESS FM REC is EPF.

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: EPF)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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