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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name bed, pediatric open hospital
510(k) Number K852422
Device Name MODEL 500 PEDIATRIC STRETCHER/CRIB
Applicant
MIDMARK CORP.
60 VISTA DR.
P.O. BOX 286
VERSAILLES,  OH  45380
Applicant Contact GENE HARSHBARGER
Correspondent
MIDMARK CORP.
60 VISTA DR.
P.O. BOX 286
VERSAILLES,  OH  45380
Correspondent Contact GENE HARSHBARGER
Regulation Number880.5140
Classification Product Code
FMS  
Date Received06/07/1985
Decision Date 07/05/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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