ClearanceBrief
510(k) K093139 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

BANTAM,48XXXXXX, 50XXXXXX

ApplicantClearStream Technologies , Ltd., Wexford, IE
DecisionSubstantially Equivalent, Dec 30, 2009
ReceivedOct 5, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093139

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.