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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stroller, Adaptive
510(k) Number K840250
Device Name CARRIER
Applicant
Convaid Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Convaid Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number890.3850
Classification Product Code
LBE  
Date Received01/11/1984
Decision Date 02/09/1984
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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