ClearanceBrief
510(k) K200269 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous

Sapphire II PRO

ApplicantOrbusneich Medical Trading, Inc., Fort Lauderdale FL, US
DecisionSubstantially Equivalent, Mar 4, 2020
ReceivedFeb 4, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K200269

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.