ClearanceBrief
510(k) K052757 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

ApplicantBiotronik AG, Lake Oswego OR, US
DecisionSubstantially Equivalent, Oct 28, 2005
ReceivedSep 30, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K052757

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.