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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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