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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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