ClearanceBrief
510(k) K921062 ยท FFX System, Gastrointestinal Motility (Electrical)

GAELTEC MPR SERIES

ApplicantMedical Measurements, Inc., Hackensack NJ, US
DecisionSubstantially Equivalent, Jul 30, 1992
ReceivedMar 5, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921062

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.