VSA 3000 VIBRATORYN SENSORY ANALYZER— 510(k) K970180

Name: FDA 510(k) clearance K970180
Creator: U.S. Food and Drug Administration
Published: 1997-04-25

Substantially Equivalent

Eare Consulting Service

FDA 510(k) clearance K970180 for VSA 3000 VIBRATORYN SENSORY ANALYZER, Substantially Equivalent on 1997-04-25. Applicant: Eare Consulting Service. Device class: 1.

Clearance details

Applicant: Eare Consulting Service
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 1997-01-17
Decision date: 1997-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eilat, IL

Download summary PDF View on FDA.gov ↗

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