ClearanceBrief
510(k) K173837 ยท DQK Computer, Diagnostic, Programmable

RHYTHMIA HDx Mapping System (with software Version 2.0)

ApplicantBoston Scientific Corporation, Cambridge MA, US
DecisionSubstantially Equivalent, Jul 25, 2018
ReceivedDec 18, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173837

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.