ClearanceBrief
510(k) K934727 ยท DWS Instruments, Surgical, Cardiovascular

REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER

ApplicantCardiac Pacemakers, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Jan 10, 1994
ReceivedOct 1, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934727

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.