Cleared Traditional

EURO TECH STERLING ROLLER TABLE

K943973 · Progressive Electrical Therapeutics · Physical Medicine
Sep 1994
Decision
45d
Days
Class 2
Risk

About This 510(k) Submission

K943973 is an FDA 510(k) clearance for the EURO TECH STERLING ROLLER TABLE, a Table, Physical Therapy, Multi Function (Class II — Special Controls, product code JFB), submitted by Progressive Electrical Therapeutics (Nevada, US). The FDA issued a Cleared decision on September 29, 1994, 45 days after receiving the submission on August 15, 1994. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.5880.

Submission Details

510(k) Number K943973 FDA.gov
FDA Decision Cleared SESE
Date Received August 15, 1994
Decision Date September 29, 1994
Days to Decision 45 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement

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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