ClearanceBrief
510(k) K203840 ยท QJP Catheter, Percutaneous, Neurovasculature

BOSS 8F Balloon Guide Catheter

ApplicantMarblehead Medical, LLC, Rochester Mn MN, US
DecisionSubstantially Equivalent, Jan 28, 2021
ReceivedDec 31, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K203840

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.