ClearanceBrief
510(k) K062308 ยท FPA Set, Administration, Intravascular

LMT-KATH-S; LMT-KATH-I

ApplicantLicher Medizintechnologie GmbH, Wedemark, DE
DecisionSubstantially Equivalent, Mar 20, 2007
ReceivedAug 8, 2006
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K062308

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.