ClearanceBrief
510(k) K862607 ยท LIO Device, Specimen Collection

IMAGEN(TM) CHLAMYDIA SPECIMEN COLLECTION KIT

ApplicantBoots-Celltech Diagnostics, Inc., Berkshire, England, GB
DecisionSubstantially Equivalent, Aug 4, 1986
ReceivedJul 8, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862607

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.