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FDA 510(k) Applications Submitted by CHELSEA PIOSKE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191305
05/14/2019
Hereaeus Poseidon Microcatheter
Heraeus Medical Components, LLC
K191502
06/06/2019
Heraeus Peripheral Guidewire
Heraeus Medical Components, LLC
K132645
08/23/2013
THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADES
MEDTRONIC, INC.
K132995
09/24/2013
DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITHOUT PRESSURE MONITORING LINE, DLP RETROGRADE CORONARY SINUS PERFUSIO
MEDTRONIC INC.
K123762
12/07/2012
DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF
MEDTRONIC INC.
K150422
02/19/2015
EOPA 3D Arterial Cannula
MEDTRONIC, INC.
K151110
04/27/2015
Intersept Filtered Cardiotomy Reservoir
Medtronic, Inc
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