Cleared Traditional

EVT-5000BX

K952600 · U.S. Table, Inc. · Physical Medicine
Jun 1995
Decision
16d
Days
Class 1
Risk

About This 510(k) Submission

K952600 is an FDA 510(k) clearance for the EVT-5000BX, a Table, Powered (Class I — General Controls, product code INQ), submitted by U.S. Table, Inc. (Glen Allen, US). The FDA issued a Cleared decision on June 22, 1995, 16 days after receiving the submission on June 6, 1995. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K952600 FDA.gov
FDA Decision Cleared SESE
Date Received June 06, 1995
Decision Date June 22, 1995
Days to Decision 16 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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