MODEL 330 SCREENING AUDIO METER, MODIFIED— 510(k) K926574

Name: FDA 510(k) clearance K926574
Creator: U.S. Food and Drug Administration
Published: 1993-03-29

Substantially Equivalent

Virtual Corp.

FDA 510(k) clearance K926574 for MODEL 330 SCREENING AUDIO METER, MODIFIED, Substantially Equivalent on 1993-03-29. Applicant: Virtual Corp.. Device class: 2.

Clearance details

Applicant: Virtual Corp.
Product code: Code GWJ
Device class: Class 2
Regulation: 21 CFR 882.1900
Advisory panel: Neurology
Date received: 1992-12-30
Decision date: 1993-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, 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.