Cleared Traditional

HI-LO TREATMENT TABLES

K933119 · Tri W-G, Inc. · Physical Medicine
Oct 1993
Decision
109d
Days
Class 1
Risk

About This 510(k) Submission

K933119 is an FDA 510(k) clearance for the HI-LO TREATMENT TABLES, 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 October 12, 1993, 109 days after receiving the submission on June 25, 1993. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K933119 FDA.gov
FDA Decision Cleared SESE
Date Received June 25, 1993
Decision Date October 12, 1993
Days to Decision 109 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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