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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Transfer, Patient, Manual
510(k) Number K871475
Device Name SOLOLIFT - PATIENT TRANSFER STRETCHER
Applicant
Adel Medical , Ltd.
16700 SE 120th Ave.
P.O. Box 542
Clackamas,  OR  97015
Applicant Contact DAVID R COLE
Correspondent
Adel Medical , Ltd.
16700 SE 120th Ave.
P.O. Box 542
Clackamas,  OR  97015
Correspondent Contact DAVID R COLE
Regulation Number880.6785
Classification Product Code
FMR  
Date Received04/14/1987
Decision Date 05/11/1987
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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