Cleared Traditional

MAT TABLE, 8100 SERIES MAT PLATFORM

K920585 · Tri W-G, Inc. · Physical Medicine
Apr 1992
Decision
57d
Days
Class 1
Risk

About This 510(k) Submission

K920585 is an FDA 510(k) clearance for the MAT TABLE, 8100 SERIES MAT PLATFORM, a Table, Powered (Class I — General Controls, product code INQ), submitted by Tri W-G, Inc. (Valley City, US). The FDA issued a Cleared decision on April 7, 1992, 57 days after receiving the submission on February 10, 1992. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K920585 FDA.gov
FDA Decision Cleared SESE
Date Received February 10, 1992
Decision Date April 07, 1992
Days to Decision 57 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF

Device Classification

Product Code INQ — Table, Powered
Device Class Class I — General Controls
CFR Regulation 21 CFR 890.3760

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