ClearanceBrief
510(k) K073623 ยท ITX Transducer, Ultrasonic, Diagnostic

ATLANTIS 018 PERIPHERAL IMAGING CATHETER

ApplicantBoston Scientific Corp, Fremont CA, US
DecisionSubstantially Equivalent, Mar 13, 2008
ReceivedDec 26, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073623

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.