AUDITORY LOCALIZER— 510(k) K811772

Name: FDA 510(k) clearance K811772
Creator: U.S. Food and Drug Administration
Published: 1981-07-15

Substantially Equivalent

Western Advanced Technology, Inc.

FDA 510(k) clearance K811772 for AUDITORY LOCALIZER, Substantially Equivalent on 1981-07-15. Applicant: Western Advanced Technology, Inc.. Device class: 2.

Clearance details

Applicant: Western Advanced Technology, Inc.
Product code: Code ETS
Device class: Class 2
Regulation: 21 CFR 874.1120
Advisory panel: Ear, Nose, Throat
Date received: 1981-06-22
Decision date: 1981-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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