ClearanceBrief
510(k) K090249 ยท DPS Electrocardiograph

MODIFICATION TO: MICRO-INDUCTION 1000 SYSTEM

ApplicantHarbinger Medical, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Apr 3, 2009
ReceivedFeb 2, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090249

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.