ClearanceBrief
510(k) K071094 ยท FFX System, Gastrointestinal Motility (Electrical)

MODIFICATION TO SOLAR GI

ApplicantMedical Measurement Systems B.V., Enschede Overijssel, NL
DecisionSubstantially Equivalent, Aug 13, 2007
ReceivedApr 18, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071094

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.