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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K760583
Device Name DISPOSABLE/BOROSILICATE CULTURE TUBES
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 Received09/03/1976
Decision Date 10/03/1976
Decision Substantially Equivalent (SESE)
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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