IN-THE-EAR MODEL 101M— 510(k) K812939

Substantially Equivalent

Danavox, Inc.

FDA 510(k) clearance K812939 for IN-THE-EAR MODEL 101M, Substantially Equivalent on 1981-11-06. Applicant: Danavox, Inc..

Clearance details

Applicant: Danavox, Inc.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1981-10-20
Decision date: 1981-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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