ClearanceBrief
510(k) K961648 ยท EJI Syringe, Cartridge

THE WAND

ApplicantSpintech, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jul 5, 1996
ReceivedApr 29, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961648

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.