ClearanceBrief
510(k) K930474 ยท FHO Pneumoperitoneum Needle

NEEDLE, PNEUMOPERITONEUM, SPRING LOADED

ApplicantRanfac, Corp., Avon MA, US
DecisionSubstantially Equivalent, Jul 23, 1993
ReceivedJan 28, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930474

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.