ClearanceBrief
510(k) K902889 ยท DTD Pacemaker Lead Adaptor

A1-A,A1-B,A1-ABP,A1-MBP,A1-Z,A6-A,A6-B,PEH PACE.

ApplicantBiotronik, GmbH & Co., Lake Oswego OR, US
DecisionSubstantially Equivalent, Aug 23, 1990
ReceivedJul 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902889

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.