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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 K792601
Device Name LIFELIFT MODELS ONE AND TWO
Applicant
Corda Int'L Holiday, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Corda Int'L Holiday, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.5510
Classification Product Code
FSA  
Date Received12/18/1979
Decision Date 12/31/1979
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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