351-AGCO BEHIND-THE-EAR HEARING AID
K-Number: K933095 · 1993-07-26
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Device Summary
Frequently Asked Questions
What is the 351-AGCO BEHIND-THE-EAR HEARING AID?
351-AGCO BEHIND-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Telex Communications, Inc.. The 510(k) number is K933095.
When did 351-AGCO BEHIND-THE-EAR HEARING AID receive FDA 510(k) clearance?
351-AGCO BEHIND-THE-EAR HEARING AID received FDA 510(k) clearance on 1993-07-26, under 510(k) number K933095.
Who is the listed applicant for 351-AGCO BEHIND-THE-EAR 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 351-AGCO BEHIND-THE-EAR HEARING AID?
The FDA product code for 351-AGCO BEHIND-THE-EAR 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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