VIBRATRON II, VIBRATION SENSITIVITY TESTER— 510(k) K863607

Name: FDA 510(k) clearance K863607
Creator: U.S. Food and Drug Administration
Published: 1986-12-03

Substantially Equivalent

Sensortek, Inc.

FDA 510(k) clearance K863607 for VIBRATRON II, VIBRATION SENSITIVITY TESTER, Substantially Equivalent on 1986-12-03. Applicant: Sensortek, Inc.. Device class: 1.

Clearance details

Applicant: Sensortek, Inc.
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 1986-09-16
Decision date: 1986-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clifton, NJ, US

Download summary PDF View on FDA.gov ↗

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