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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Wheelchair, Powered
510(k) Number K881463
Device Name MULTIMODE(TM) POWER MODULE SYSTEM
Applicant
Dufco Electronics, Inc.
2535-C Village Ln.
Cambria,  CA  93428
Applicant Contact PETER A DUFRESNE
Correspondent
Dufco Electronics, Inc.
2535-C Village Ln.
Cambria,  CA  93428
Correspondent Contact PETER A DUFRESNE
Regulation Number890.3860
Classification Product Code
ITI  
Date Received04/07/1988
Decision Date 07/18/1988
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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