Cleared Traditional

TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777

K960196 · Tri W-G, Inc. · Physical Medicine
Feb 1996
Decision
22d
Days
Class 1
Risk

About This 510(k) Submission

K960196 is an FDA 510(k) clearance for the TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777, 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 February 7, 1996, 22 days after receiving the submission on January 16, 1996. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K960196 FDA.gov
FDA Decision Cleared SESE
Date Received January 16, 1996
Decision Date February 07, 1996
Days to Decision 22 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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