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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Mechanical
510(k) Number K894987
Device Name MODEL #520/525 ED/RECOVERY STRETCHER
Applicant
MEDMARK, INC.
VERSAILLES,  OH  45380
Applicant Contact JOHN OLDIGES
Correspondent
MEDMARK, INC.
VERSAILLES,  OH  45380
Correspondent Contact JOHN OLDIGES
Regulation Number890.3750
Classification Product Code
INW  
Date Received08/08/1989
Decision Date 09/05/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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