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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 K930625
Device Name SANITAS PATIENT LIFT
Applicant
Dutton-Lainson Co.
451 W. Second St.
Hastings,  NE  68902
Applicant Contact RON HAASE
Correspondent
Dutton-Lainson Co.
451 W. Second St.
Hastings,  NE  68902
Correspondent Contact RON HAASE
Regulation Number880.5510
Classification Product Code
FSA  
Date Received02/08/1993
Decision Date 09/13/1993
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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