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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, Ac-Powered
510(k) Number K895677
Device Name THE MURRAY MOBILIFT(TM)
Applicant
Medical/Surgical Specialties, Ltd.
1611 W. Centre St.
Kalamazoo,  MI  49002
Applicant Contact JAMES L PHILLIPS
Correspondent
Medical/Surgical Specialties, Ltd.
1611 W. Centre St.
Kalamazoo,  MI  49002
Correspondent Contact JAMES L PHILLIPS
Regulation Number880.5500
Classification Product Code
FNG  
Date Received09/20/1989
Decision Date 10/26/1990
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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