ClearanceBrief
510(k) K143093 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

0.018 Arrow GPSCath Balloon Dilatation Catheter (150 cm)

ApplicantHotspur Technologies, Inc.,, Mountain View CA, US
DecisionSubstantially Equivalent, Jun 24, 2015
ReceivedOct 28, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K143093

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.