ClearanceBrief
510(k) K833814 ยท LIO Device, Specimen Collection

SANI CATCH BA

ApplicantConcord Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 19, 1984
ReceivedNov 2, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833814

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.