ClearanceBrief
510(k) K922683 ยท EJI Syringe, Cartridge

PRESTYL JET INJECTOR

ApplicantBma Technologies S.A., Washington DC, US
DecisionSubstantially Equivalent, Apr 11, 1994
ReceivedJun 4, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922683

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.