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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 K935351
Device Name A.C. POWER PATIENT LIFT
Applicant
Ken Kemmerer
788 Keating St.
Wilkes Barre Twp,  PA  18702
Applicant Contact KEN KEMMERER
Correspondent
Ken Kemmerer
788 Keating St.
Wilkes Barre Twp,  PA  18702
Correspondent Contact KEN KEMMERER
Regulation Number880.5500
Classification Product Code
FNG  
Date Received11/05/1993
Decision Date 02/28/1994
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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