TELEX MODEL 28A ITE CUSTOM HEARING AID
K-Number: K922066 · 1992-05-18
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Device Summary
Frequently Asked Questions
What is the TELEX MODEL 28A ITE CUSTOM HEARING AID?
TELEX MODEL 28A ITE CUSTOM HEARING AID is a medical device that received FDA 510(k) clearance on 1992-05-18. The listed applicant is Telex Communications, Inc.. The 510(k) number is K922066.
When did TELEX MODEL 28A ITE CUSTOM HEARING AID receive FDA 510(k) clearance?
TELEX MODEL 28A ITE CUSTOM HEARING AID received FDA 510(k) clearance on 1992-05-18, under 510(k) number K922066.
Who is the listed applicant for TELEX MODEL 28A ITE CUSTOM 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 TELEX MODEL 28A ITE CUSTOM HEARING AID?
The FDA product code for TELEX MODEL 28A ITE CUSTOM 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.
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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