ClearanceBrief
510(k) K130785 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)

SEER 1000

ApplicantGetemed Medizin- Und Informationstechnik AG, Teltow, DE
DecisionSubstantially Equivalent, Jul 26, 2013
ReceivedMar 21, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K130785

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.