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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 K870226
Device Name PERMOBIL MINIOR
Applicant
Permobil of America
Box 20
1644 Massachusetts Ave.
Lexington,  MA  02173
Applicant Contact FINKELSTEIN, MD
Correspondent
Permobil of America
Box 20
1644 Massachusetts Ave.
Lexington,  MA  02173
Correspondent Contact FINKELSTEIN, MD
Regulation Number890.3860
Classification Product Code
ITI  
Date Received01/21/1987
Decision Date 02/10/1987
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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