ClearanceBrief
510(k) K083749 ยท LOS

CARDIOVIEW32 REVIEW MODULE

ApplicantQrs Diagnostic, LLC, Plymouth MN, US
DecisionSubstantially Equivalent, Mar 10, 2009
ReceivedDec 17, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083749

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.