ClearanceBrief
510(k) K102329 ยท OAB Low Energy Direct Current Thermal Ablation System

NANOKNIFE SYSTEM

ApplicantAngioDynamics, Inc., Sunnyvale CA, US
DecisionSubstantially Equivalent, Oct 24, 2011
ReceivedAug 17, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K102329

DateFirm and productCodeLinked 510(k)
Jan 27, 2012Angiodynamics Worldwide Headquarters
NanoKnife Irreversible Electroporation System. System consists of multiple components: Generator, footswitch, disposable electrode. System is manufactured by AngioDynamics, Inc. --- Catalog #20300101
Terminated
OABNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.