FDA 510(k) Applications Submitted by CHARLES DENAULT

FDA 510(k) Number Submission Date Device Name Applicant
K160832 03/25/2016 Penumbra Smart Coil PENUMBRA, INC.
K161064 04/15/2016 Penumbra System ACE 68 Reperfusion Catheter Penumbra, Inc.
K141134 05/01/2014 POD SYSTEM PENUMBRA, INC.
K151572 06/11/2015 Penumbra Smart Coil PENUMBRA, INC.
K161640 06/14/2016 Penumbra System ACE 68 Reperfusion Catheter Penumbra, Inc.
K152840 09/29/2015 Lantern Delivery Microcatheter PENUMBRA, INC.
K143218 11/10/2014 Penumbra Smart Coil Penumbra, Inc.


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