ClearanceBrief
510(k) K930313 ยท LIO Device, Specimen Collection

APEX SPECIMEN BAG

ApplicantApex Medical Technologies, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Mar 18, 1993
ReceivedJan 22, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930313

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.