Cleared Traditional

CARDON PHYSICAL THERAPY TABLE MODEL:R40194

K951955 · Cardon Rehabilitation Products, Inc. · Physical Medicine
Jun 1995
Decision
57d
Days
Class 1
Risk

About This 510(k) Submission

K951955 is an FDA 510(k) clearance for the CARDON PHYSICAL THERAPY TABLE MODEL:R40194, a Table, Powered (Class I — General Controls, product code INQ), submitted by Cardon Rehabilitation Products, Inc. (Niagara Falls, US). The FDA issued a Cleared decision on June 22, 1995, 57 days after receiving the submission on April 26, 1995. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K951955 FDA.gov
FDA Decision Cleared SESE
Date Received April 26, 1995
Decision Date June 22, 1995
Days to Decision 57 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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