TINNITUS MASKERS MODEL S584— 510(k) K790190

Name: FDA 510(k) clearance K790190
Creator: U.S. Food and Drug Administration
Published: 1979-02-12

Substantially Equivalent

Vican Instrument Co.

FDA 510(k) clearance K790190 for TINNITUS MASKERS MODEL S584, Substantially Equivalent on 1979-02-12. Applicant: Vican Instrument Co.. Device class: 2.

Clearance details

Applicant: Vican Instrument Co.
Product code: Code KLW
Device class: Class 2
Regulation: 21 CFR 874.3400
Advisory panel: Ear, Nose, Throat
Date received: 1979-01-26
Decision date: 1979-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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