ClearanceBrief
510(k) K191229 ยท DQY Catheter, Percutaneous

TrapIt

ApplicantImds Operations B.V., Roden, NL
DecisionSubstantially Equivalent, Jan 21, 2020
ReceivedMay 8, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191229

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.