ClearanceBrief
510(k) K192246 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

Biowy PICC Catheter S Kit

ApplicantBiowy Corporation, Lake Forest CA, US
DecisionSubstantially Equivalent, Apr 30, 2020
ReceivedAug 19, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192246

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.