ClearanceBrief
510(k) K903401 ยท HAE Rongeur, Manual

SPECIAL RONGEUR

ApplicantSur-Med Instruments, Inc., St. Louis MO, US
DecisionSubstantially Equivalent, Aug 10, 1990
ReceivedJul 31, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903401

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.