ClearanceBrief
510(k) K000482 ยท KZH Introducer, Syringe Needle

MODIFICATION TO AUTOJECT MINI

ApplicantOwen Mumford, Ltd., Marietta GA, US
DecisionSubstantially Equivalent, Mar 6, 2000
ReceivedFeb 14, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000482

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.