Cleared Traditional

CARDON PHYSICAL THERAPY TABLE MODEL R27645

K960336 · Cardon Rehabilitation Products, Inc. · Physical Medicine
Feb 1996
Decision
20d
Days
Class 1
Risk

About This 510(k) Submission

K960336 is an FDA 510(k) clearance for the CARDON PHYSICAL THERAPY TABLE MODEL R27645, 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 February 13, 1996, 20 days after receiving the submission on January 24, 1996. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K960336 FDA.gov
FDA Decision Cleared SESE
Date Received January 24, 1996
Decision Date February 13, 1996
Days to Decision 20 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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