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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: 01/16/2017
 
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aortic root cannula DLP, INC. K790565 06/11/1979
aortic root cannula w/integral press DLP, INC. K831591 06/30/1983
arterial cannula curved beveled tip DLP, INC. K840002 02/13/1984
arterial cannula straight beveled tip DLP, INC. K840001 02/13/1984
aspirating needle, catalog code #12006 DLP, INC. K865079 03/03/1987
cardiopulminary bypass catheter cannula DLP, INC. K810548 03/17/1981
cardiopulmonary bypass DLP, INC. K810820 04/03/1981
catheter two stage venous return DLP, INC. K915268 07/27/1992
code #94315 retrograde coronary sinus perf cannula DLP, INC. K901074 07/06/1990
descending arch cannula DLP, INC. K880421 04/28/1988
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