ClearanceBrief
510(k) K142901 ยท DQK Computer, Diagnostic, Programmable

RhythmView Workstation

ApplicantTopera, Inc., St.Louis MO, US
DecisionSubstantially Equivalent, Dec 19, 2014
ReceivedOct 14, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K142901

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.