ClearanceBrief
510(k) K180443 ยท NEU Marker, Radiographic, Implantable

Tumark Vision

ApplicantSomatex Medical Technologies GmbH, Teltow, DE
DecisionSubstantially Equivalent, Mar 22, 2018
ReceivedFeb 20, 2018
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K180443

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.