ClearanceBrief
510(k) K880342 ยท FMF Syringe, Piston

UROSTHESIA

ApplicantMedical Research Innovators, Inc., El Cajon CA, US
DecisionSubstantially Equivalent, Feb 25, 1988
ReceivedJan 26, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880342

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.