ClearanceBrief
510(k) K190318 ยท DXC Clamp, Vascular

VASOBand Vascular Compression Device

ApplicantVasoinnovations, Inc., South Pasadena CA, US
DecisionSubstantially Equivalent, Mar 14, 2019
ReceivedFeb 13, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190318

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.