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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 K854120
Device Name MURRAY CHAIR LIFT
Applicant
J.B. Murray Enterprises, Inc.
301 E. Kalamazoo St.
P.O. Box 145
Bloomingdale,  MI  49026
Applicant Contact CHARLES WILSON
Correspondent
J.B. Murray Enterprises, Inc.
301 E. Kalamazoo St.
P.O. Box 145
Bloomingdale,  MI  49026
Correspondent Contact CHARLES WILSON
Regulation Number880.5500
Classification Product Code
FNG  
Date Received10/09/1985
Decision Date 11/01/1985
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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