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FDA 510(k)

TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER

K-Number: K915397 · 1992-01-17

Decision Date1992-01-17
Product CodeEPF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER 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 1992-01-17 under 510(k) number K915397. 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 TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER?

TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Telex Communications, Inc.. The 510(k) number is K915397.

When did TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER receive FDA 510(k) clearance?

TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER received FDA 510(k) clearance on 1992-01-17, under 510(k) number K915397.

Who is the listed applicant for TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER?

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 TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER?

The FDA product code for TDR-7 BINAURAL HEARING AID/WIRELESS FM RECIEVER 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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