ClearanceBrief
510(k) K983325 ยท FEN Device, Cystometric, Hydraulic

IN-PROBE II URODYNAMIC SYSTEM

ApplicantInfluence, Inc., San Francisco CA, US
DecisionSubstantially Equivalent, Nov 24, 1998
ReceivedSep 22, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983325

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.