Cleared Traditional

LIC-ORTHION MULTI-THERAPY TREATMENT TABLE

K862022 · Lic-Orthion · Physical Medicine
Jun 1986
Decision
22d
Days
Class 2
Risk

About This 510(k) Submission

K862022 is an FDA 510(k) clearance for the LIC-ORTHION MULTI-THERAPY TREATMENT TABLE, a Table, Physical Therapy, Multi Function (Class II — Special Controls, product code JFB), submitted by Lic-Orthion (Washington, US). The FDA issued a Cleared decision on June 19, 1986, 22 days after receiving the submission on May 28, 1986. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.5880.

Submission Details

510(k) Number K862022 FDA.gov
FDA Decision Cleared SESE
Date Received May 28, 1986
Decision Date June 19, 1986
Days to Decision 22 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary —

Device Classification

Product Code JFB — Table, Physical Therapy, Multi Function
Device Class Class II — Special Controls
CFR Regulation 21 CFR 890.5880

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