ClearanceBrief
510(k) K822344 ยท LJF Device, Antimicrobial Drug Removal

ANTIMICROBIAL REMOVAL DEVICE (ARD)

ApplicantMarion Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 25, 1982
ReceivedAug 5, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822344

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.