ClearanceBrief
510(k) K934141 ยท FEN Device, Cystometric, Hydraulic

STAND ALONE CYSTOMETROGRAM

ApplicantMedical Engineering Corp., Racine WI, US
DecisionSubstantially Equivalent, Nov 18, 1993
ReceivedAug 25, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934141

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.