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

Substantially Equivalent

Sensortek, Inc.

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

Clearance details

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

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