ClearanceBrief
510(k) K863681 ยท LJP Antiserum, Fluorescent, Chlamydia Trachomatis

PATHFINDER(TM) DIRECT ANTIGEN DETECTION SYSTEM

ApplicantKallestad Laboratories, Inc., Chaska MN, US
DecisionSubstantially Equivalent, Dec 3, 1986
ReceivedSep 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863681

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.