ClearanceBrief
510(k) K911827 ยท DTD Pacemaker Lead Adaptor

MODEL 5866-9M & MODEL 6981M

ApplicantMetronic, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jul 23, 1991
ReceivedApr 24, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911827

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.