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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K842685
Device Name BECTON DICKINSON 1000 INSULIN PUMP
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
1875 Eye St. NW Suite 625
Washington,  DC  20006
Correspondent
Bd Becton Dickinson Vacutainer Systems Preanalytic
1875 Eye St. NW Suite 625
Washington,  DC  20006
Date Received07/10/1984
Decision Date 07/10/1984
Decision SE - Postmarket Surveillance Required (SESP)
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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