Cleared Traditional

MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE

K925594 · Tri W-G, Inc. · Physical Medicine
Feb 1993
Decision
99d
Days
Class 1
Risk

About This 510(k) Submission

K925594 is an FDA 510(k) clearance for the MDL 29001 MEDI ELEC-MECH 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 February 12, 1993, 99 days after receiving the submission on November 5, 1992. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K925594 FDA.gov
FDA Decision Cleared SESE
Date Received November 05, 1992
Decision Date February 12, 1993
Days to Decision 99 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement

Device Classification

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

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