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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 K851844
Device Name MOLIFT
Applicant
MADSHUS A/S
2820 BIRI
BIRI,  NO
Applicant Contact OYUIND B TORP
Correspondent
MADSHUS A/S
2820 BIRI
BIRI,  NO
Correspondent Contact OYUIND B TORP
Regulation Number880.5510
Classification Product Code
FSA  
Date Received04/26/1985
Decision Date 05/17/1985
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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