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FDA 510(k)

TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION

K-Number: K963915 · 1996-11-08

Decision Date1996-11-08
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION 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 1996-11-08 under 510(k) number K963915. 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 TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION?

TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION is a medical device that received FDA 510(k) clearance on 1996-11-08. The listed applicant is Telex Communications, Inc.. The 510(k) number is K963915.

When did TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION receive FDA 510(k) clearance?

TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION received FDA 510(k) clearance on 1996-11-08, under 510(k) number K963915.

Who is the listed applicant for TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION?

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 IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION?

The FDA product code for TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION 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

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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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