ClearanceBrief
510(k) K181852 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Percuvance Percutaneous Surgical System

ApplicantTeleflexmedical, Inc., Morrisville NC, US
DecisionSubstantially Equivalent, Oct 12, 2018
ReceivedJul 11, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181852

No recall in the FDA data names this 510(k).

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