DFS GENIUS BTE
K-Number: K924185 · 1992-11-03
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Device Summary
Frequently Asked Questions
What is the DFS GENIUS BTE?
DFS GENIUS BTE is a medical device that received FDA 510(k) clearance on 1992-11-03. The listed applicant is Gn Danavox, Inc.. The 510(k) number is K924185.
When did DFS GENIUS BTE receive FDA 510(k) clearance?
DFS GENIUS BTE received FDA 510(k) clearance on 1992-11-03, under 510(k) number K924185.
Who is the listed applicant for DFS GENIUS BTE?
The FDA 510(k) record lists Gn Danavox, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DFS GENIUS BTE?
The FDA product code for DFS GENIUS BTE 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 Gn Danavox, 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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