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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 K860837
Device Name HOYER ONE-TOUCH POWER LIFTER
Applicant
TED HOYER & CO., INC.
2222 MINNESOTA ST.
P.O. BOX 2744
OSHKOSH,  WI  54903
Applicant Contact S. C SCHUPPE
Correspondent
TED HOYER & CO., INC.
2222 MINNESOTA ST.
P.O. BOX 2744
OSHKOSH,  WI  54903
Correspondent Contact S. C SCHUPPE
Regulation Number880.5510
Classification Product Code
FSA  
Date Received03/05/1986
Decision Date 03/27/1986
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
Recalls CDRH Recalls
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