TELEX MODEL TLP, IN-THE-EAR
K-Number: K912204 · 1991-06-20
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Device Summary
Frequently Asked Questions
What is the TELEX MODEL TLP, IN-THE-EAR?
TELEX MODEL TLP, IN-THE-EAR is a medical device that received FDA 510(k) clearance on 1991-06-20. The listed applicant is Telex Communications, Inc.. The 510(k) number is K912204.
When did TELEX MODEL TLP, IN-THE-EAR receive FDA 510(k) clearance?
TELEX MODEL TLP, IN-THE-EAR received FDA 510(k) clearance on 1991-06-20, under 510(k) number K912204.
Who is the listed applicant for TELEX MODEL TLP, IN-THE-EAR?
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 TLP, IN-THE-EAR?
The FDA product code for TELEX MODEL TLP, IN-THE-EAR 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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