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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pump, Infusion
510(k) Number K832641
Device Name WINDSOR MEDICAL MODEL 52
Applicant
Windsor Medical, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Windsor Medical, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.5725
Classification Product Code
FRN  
Date Received08/04/1983
Decision Date 10/04/1983
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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