Cleared Traditional

MODELS 642 & 643 TILT EXAM/TREATMENT TABLE

K930802 · Tri W-G, Inc. · Physical Medicine
Mar 1993
Decision
34d
Days
Class 1
Risk

About This 510(k) Submission

K930802 is an FDA 510(k) clearance for the MODELS 642 & 643 TILT EXAM/TREATMENT TABLE, 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 March 22, 1993, 34 days after receiving the submission on February 16, 1993. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K930802 FDA.gov
FDA Decision Cleared SESE
Date Received February 16, 1993
Decision Date March 22, 1993
Days to Decision 34 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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