ClearanceBrief
510(k) K864539 ยท LJP Antiserum, Fluorescent, Chlamydia Trachomatis

MODIFIED IMAGEN(TM) CHLAMYDIA TEST

ApplicantBoots-Celltech Diagnostics, Inc., Berkshire, England, GB
DecisionSubstantially Equivalent, Mar 12, 1987
ReceivedNov 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864539

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.