ClearanceBrief
510(k) K231626 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

OSPREY Closed IV Catheter System (OspreyV2)

ApplicantSkydance Vascular, Inc., Pleasant Grove UT, US
DecisionSubstantially Equivalent, Aug 31, 2023
ReceivedJun 2, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231626

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.