ClearanceBrief
510(k) K203803 ยท DXC Clamp, Vascular

VASOBand Vascular Compression Device

ApplicantVasoinnovations, Inc., South Pasadena CA, US
DecisionSubstantially Equivalent, Jan 26, 2021
ReceivedDec 28, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203803

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.