ClearanceBrief
510(k) K082249 ยท EJI Syringe, Cartridge

MORPHEUS

ApplicantMeibach Tech Ltda, New York NY, US
DecisionSubstantially Equivalent, Dec 31, 2009
ReceivedAug 8, 2008
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K082249

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.