ClearanceBrief
510(k) K201794 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

Jade

ApplicantOrbusNeich Medical (Shenzhen) Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Jul 28, 2020
ReceivedJun 30, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K201794

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.