TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION
K-Number: K963915 · 1996-11-08
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Device Summary
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.
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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