ClearanceBrief
510(k) K210358 ยท MJN Catheter, Intravascular Occluding, Temporary

Neurescue device

ApplicantNeurescue Aps, Copenhagen, DK
DecisionSubstantially Equivalent, May 21, 2021
ReceivedFeb 8, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210358

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.