ClearanceBrief
510(k) K250292 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

OSPREY Midline Closed IV Catheter System (OspreyEDC-F20)

ApplicantSkydance Vascular, Inc., Pleasant Grove UT, US
DecisionSubstantially Equivalent, May 2, 2025
ReceivedJan 31, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250292

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.