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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Powered
510(k) Number K943972
Device Name EURO TECH DIAMOND CHIROPRACTIC TABLE
Applicant
Progressive Electrical Therapeutics
200 S. Alma
Nevada,  MO  64772
Applicant Contact GARY HUDDLESTON
Correspondent
Progressive Electrical Therapeutics
200 S. Alma
Nevada,  MO  64772
Correspondent Contact GARY HUDDLESTON
Regulation Number890.3760
Classification Product Code
INQ  
Date Received08/15/1994
Decision Date 10/11/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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