ClearanceBrief
510(k) K991680 ยท KZH Introducer, Syringe Needle

SOFTINJECT

ApplicantAndrosystems Srl, Rome, IT
DecisionSubstantially Equivalent, Jun 3, 1999
ReceivedMay 17, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991680

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.