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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 22 Results
ProductCode: DWF Applicant: DLP, INC Decision Date To: 08/28/2016
 
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510(K)
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aortic root cannula DLP, INC. K790565 06/11/1979
cardiopulminary bypass catheter cannula DLP, INC. K810548 03/17/1981
cardiopulmonary bypass DLP, INC. K810820 04/03/1981
submission coronary cannula DLP, INC. K821149 05/18/1982
aortic root cannula w/integral press DLP, INC. K831591 06/30/1983
infant vent catheter 12001 w/side vent DLP, INC. K834039 01/03/1984
arterial cannula curved beveled tip DLP, INC. K840002 02/13/1984
arterial cannula straight beveled tip DLP, INC. K840001 02/13/1984
pressure catheter placement set 50010 DLP, INC. K841482 06/11/1984
pul,monary artery vent catheter DLP, INC. K845046 04/03/1985
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