WIDEX MODEL SENSO DIGITAL (C9)— 510(k) K965254

Substantially Equivalent

Widex Hearing Aid Co., Inc.

FDA 510(k) clearance K965254 for WIDEX MODEL SENSO DIGITAL (C9), Substantially Equivalent on 1997-03-12. Applicant: Widex Hearing Aid Co., Inc..

Clearance details

Applicant: Widex Hearing Aid Co., Inc.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1996-12-30
Decision date: 1997-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island City, NY, US

Download summary PDF View on FDA.gov ↗

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