ClearanceBrief
510(k) K771986 ยท FHF System, Evacuator, Fluid

CATHETER, MEDIASTINAL&PERICARDIAL

ApplicantThe Minnesota Back Brace Co., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 28, 1977
ReceivedOct 19, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K771986

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.