ClearanceBrief
510(k) K913541 ยท FMF Syringe, Piston

NEO-THOR THORACOSTOMY KIT

ApplicantIntl. Medical Devices , Ltd., Los Angeles CA, US
DecisionSubstantially Equivalent, Apr 9, 1992
ReceivedAug 9, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913541

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.