ClearanceBrief
510(k) K874709 ยท FFT Electrode, Ph, Stomach

DIAMOND MEDICAL, INC. MODEL DM 800

ApplicantDiamond Medical, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Feb 8, 1988
ReceivedNov 12, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874709

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.