ClearanceBrief
510(k) K970204 ยท DTD Pacemaker Lead Adaptor

BK-A; BK-B; BK-IS SEALING CAP

ApplicantBiotronik, Inc., Lake Oswego OR, US
DecisionSubstantially Equivalent, Apr 29, 1997
ReceivedJan 21, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970204

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.