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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lift, Patient, Non-Ac-Powered
510(k) Number K840997
Device Name BATTERY POWERED PATIENT LIFT
Applicant
Invacare Corp.
One Invacare Way
P.O. Box 4028
Elyria,  OH  44036
Correspondent
Invacare Corp.
One Invacare Way
P.O. Box 4028
Elyria,  OH  44036
Regulation Number880.5510
Classification Product Code
FSA  
Date Received03/08/1984
Decision Date 04/17/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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