ClearanceBrief
510(k) K212211 ยท DQY Catheter, Percutaneous

Turnpike catheter, Turnpike Spiral catheter, Turnpike LP catheter, Turnpike Gold catheter, GuideLiner V3 catheter, TrapLiner catheter

ApplicantVascular Solutions, LLC, Minneapolis MN, US
DecisionSubstantially Equivalent, Feb 9, 2022
ReceivedJul 15, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212211

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.