ClearanceBrief
510(k) K983925 ยท HIF Insufflator, Laparoscopic

ENDOPATH ULTRA VERESS NEEDLE

ApplicantEthicon Endo-Surgery, Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, Feb 3, 1999
ReceivedNov 5, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983925

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.