MODEL 339 TELECROS WIRELESS BICROS
K-Number: K792462 · 1980-01-09
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Device Summary
Frequently Asked Questions
What is the MODEL 339 TELECROS WIRELESS BICROS?
MODEL 339 TELECROS WIRELESS BICROS is a medical device that received FDA 510(k) clearance on 1980-01-09. The listed applicant is Telex Communications, Inc.. The 510(k) number is K792462.
When did MODEL 339 TELECROS WIRELESS BICROS receive FDA 510(k) clearance?
MODEL 339 TELECROS WIRELESS BICROS received FDA 510(k) clearance on 1980-01-09, under 510(k) number K792462.
Who is the listed applicant for MODEL 339 TELECROS WIRELESS BICROS?
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 MODEL 339 TELECROS WIRELESS BICROS?
The FDA product code for MODEL 339 TELECROS WIRELESS BICROS 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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