Cleared Traditional

CARDON PHYSICAL THERAPY TABLE MODEL R27112

K951952 · Cardon Rehabilitation Products, Inc. · Physical Medicine
May 1995
Decision
35d
Days
Class 1
Risk

About This 510(k) Submission

K951952 is an FDA 510(k) clearance for the CARDON PHYSICAL THERAPY TABLE MODEL R27112, 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 May 31, 1995, 35 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 K951952 FDA.gov
FDA Decision Cleared SESE
Date Received April 26, 1995
Decision Date May 31, 1995
Days to Decision 35 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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