ClearanceBrief
510(k) K833199 ยท DXY Implantable Pacemaker Pulse-Generator

SILICONE RUBBER ISOLATION SLEEVE 350-01

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 28, 1983
ReceivedSep 19, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833199

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.