Cleared Traditional

K872093 - RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING
(FDA 510(k) Clearance)

Sep 1987
Decision
107d
Days
Risk

K872093 is an FDA 510(k) clearance for the RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING. This device is classified as a Apparatus, Vestibular Analysis.

Submitted by Ics Medical Corp. (Schaumburg, US). The FDA issued a Cleared decision on September 16, 1987, 107 days after receiving the submission on June 1, 1987.

This device falls under the Ear, Nose, Throat FDA review panel.

Submission Details

510(k) Number K872093 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 01, 1987
Decision Date September 16, 1987
Days to Decision 107 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary

Device Classification

Product Code LXV — Apparatus, Vestibular Analysis
Device Class