ClearanceBrief
510(k) K241025 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

JADE PLUS PTA Balloon Dilatation Catheter

ApplicantOrbusNeich Medical (Shenzhen) Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Jun 11, 2024
ReceivedApr 15, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241025

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.