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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 K885270
Device Name PERSONAL TRANSFER SYSTEM
Applicant
Columbus Mckinnon Corp.
Tonawanda Operations
One Fremont St.
Tonawanda,  NY  14151
Applicant Contact EARL L LOESWICK
Correspondent
Columbus Mckinnon Corp.
Tonawanda Operations
One Fremont St.
Tonawanda,  NY  14151
Correspondent Contact EARL L LOESWICK
Regulation Number880.5500
Classification Product Code
FNG  
Date Received12/22/1988
Decision Date 03/14/1989
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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