Cleared Traditional

EURO TECH DIAMOND CHIROPRACTIC TABLE

K943972 · Progressive Electrical Therapeutics · Physical Medicine
Oct 1994
Decision
57d
Days
Class 1
Risk

About This 510(k) Submission

K943972 is an FDA 510(k) clearance for the EURO TECH DIAMOND CHIROPRACTIC TABLE, a Table, Powered (Class I — General Controls, product code INQ), submitted by Progressive Electrical Therapeutics (Nevada, US). The FDA issued a Cleared decision on October 11, 1994, 57 days after receiving the submission on August 15, 1994. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K943972 FDA.gov
FDA Decision Cleared SESE
Date Received August 15, 1994
Decision Date October 11, 1994
Days to Decision 57 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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