ClearanceBrief
510(k) K823536 ยท EJI Syringe, Cartridge

INTRALIG

ApplicantMiltex Instrument Co., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 28, 1982
ReceivedNov 30, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823536

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.