FDA 510(k) Applications Submitted by Lydia Sakakeeny

FDA 510(k) Number Submission Date Device Name Applicant
K170296 01/31/2017 CoreCath 2.7S Medtronic Advanced Energy
K150297 02/06/2015 PlasmaBlade UPPP and Suction Coagulator MEDTRONIC ADVANCED ENERGY
K170610 03/01/2017 PlasmaBlade T Medtronic Advanced Energy
K110980 04/07/2011 CENTRIMAG RETURN CANNULA KIT LEVITRONIX LLC.
K110983 04/07/2011 CENTRIMAG DRAINAGE CANNULA KIT LEVITRONIX LLC
K152703 09/21/2015 PlasmaBlade TnA Tonsil and Adenoid Dissection Device MEDTRONIC ADVANCED ENERGY


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