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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Wheeled
510(k) Number K943969
Device Name MODEL 578 MOBILE SURGICAL STRETCHER
Applicant
Hausted, Inc.
927 Lake Rd.
P.O. Box 710
Medina,  OH  44258
Applicant Contact RAYMOND A FAILOR
Correspondent
Hausted, Inc.
927 Lake Rd.
P.O. Box 710
Medina,  OH  44258
Correspondent Contact RAYMOND A FAILOR
Regulation Number880.6910
Classification Product Code
FPO  
Date Received08/15/1994
Decision Date 01/25/1995
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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