ClearanceBrief
510(k) K844619 ยท FHO Pneumoperitoneum Needle

ENDONEEDLE

ApplicantEndotherapeutics, Redwood City CA, US
DecisionSubstantially Equivalent, Jan 9, 1985
ReceivedNov 27, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844619

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.