OCTOTOXIC SCREENER— 510(k) K811790

Name: FDA 510(k) clearance K811790
Creator: U.S. Food and Drug Administration
Published: 1981-07-15

Substantially Equivalent

Western Advanced Technology, Inc.

FDA 510(k) clearance K811790 for OCTOTOXIC SCREENER, 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: 1981-06-24
Decision date: 1981-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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