ClearanceBrief
510(k) K993147 ยท FPA Set, Administration, Intravascular

DECAP

ApplicantThe Kipp Group, Ontario CA, US
DecisionSubstantially Equivalent, Nov 2, 1999
ReceivedSep 21, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993147

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.