ClearanceBrief
510(k) K082472 ยท LIO Device, Specimen Collection

VIROCULT, MODEL MW950

ApplicantMedical Wire & Equipment Company (Bath), Ltd., Corsham, Wiltshire, GB
DecisionSubstantially Equivalent, Dec 30, 2008
ReceivedAug 28, 2008
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K082472

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.