TINNITUS MASKERS, MODELS S564&S574— 510(k) K771769

Name: FDA 510(k) clearance K771769
Creator: U.S. Food and Drug Administration
Published: 1978-01-03

Substantially Equivalent

Vicon Instrument Co.

FDA 510(k) clearance K771769 for TINNITUS MASKERS, MODELS S564&S574, Substantially Equivalent on 1978-01-03. Applicant: Vicon Instrument Co.. Device class: 2.

Clearance details

Applicant: Vicon Instrument Co.
Product code: Code KLW
Device class: Class 2
Regulation: 21 CFR 874.3400
Advisory panel: Ear, Nose, Throat
Date received: 1977-09-19
Decision date: 1978-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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