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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 K854058
Device Name PK-AC POWERED PATIENT MANUPULATING DEVICE
Applicant
Mannesmann Demag Corp.
29201 Aurora Rd.
P.O. Box 39245
Solon,  OH  44139
Applicant Contact DAVID R MARSHALL
Correspondent
Mannesmann Demag Corp.
29201 Aurora Rd.
P.O. Box 39245
Solon,  OH  44139
Correspondent Contact DAVID R MARSHALL
Regulation Number880.5500
Classification Product Code
FNG  
Date Received10/03/1985
Decision Date 02/25/1986
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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