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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 24 Results
ProductCode: FMF Applicant: BD Decision Date To: 10/25/2014
 
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510(K)
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bd integra syringe bd K023752 02/07/2003
bd single lumen needle, syringe and bloo bd K021475 07/19/2002
bd spring based syringe bd K011103 06/13/2001
sterile water for injection prefilled sy bd becton dickinson vacutainer systems p K972728 07/15/1998
becton dickinson syringes bd becton dickinson vacutainer systems p K980580 06/25/1998
b-d pen ultra bd becton dickinson vacutainer systems p K981797 06/12/1998
becton dickinson syringe bd becton dickinson vacutainer systems p K980987 06/11/1998
b-d e ml pen bd becton dickinson vacutainer systems p K980755 04/02/1998
becton dickinson syringse bd becton dickinson vacutainer systems p K954064 11/21/1995
b-d pen ultra bd becton dickinson vacutainer systems p K951919 10/24/1995
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