ClearanceBrief
510(k) K180222 ยท JXI Cuff, Nerve

Reaxon Plus

ApplicantMedovent GmbH, Mainz, DE
DecisionSubstantially Equivalent, Apr 24, 2018
ReceivedJan 25, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180222

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.