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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Patient Transfer, Powered
510(k) Number K910830
Device Name INVALIFT
Applicant
American Invalift Corp.
285 Tarrytown Rd.
White Plains,  NY  10607
Applicant Contact THERESE RUBINO
Correspondent
American Invalift Corp.
285 Tarrytown Rd.
White Plains,  NY  10607
Correspondent Contact THERESE RUBINO
Regulation Number880.6775
Classification Product Code
FRZ  
Date Received02/27/1991
Decision Date 06/09/1992
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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