DFS GENIUS BTE— 510(k) K924185

Substantially Equivalent

Gn Danavox, Inc.

FDA 510(k) clearance K924185 for DFS GENIUS BTE, Substantially Equivalent on 1992-11-03. Applicant: Gn Danavox, Inc..

Clearance details

Applicant: Gn Danavox, Inc.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1992-08-20
Decision date: 1992-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.