ClearanceBrief
510(k) K242969 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous

Pantera Pro; Pantera LEO

ApplicantBiotronik, Inc., Lake Oswego OR, US
DecisionSubstantially Equivalent, Oct 25, 2024
ReceivedSep 26, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K242969

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.