ClearanceBrief
510(k) K893669 ยท LKH Antisera, Immunoperoxidase, Chlamydia Spp.

CELLMATICS SHLAMYDIA DETECTION SYSTEM

ApplicantDifco Laboratories, Inc., Detroit MI, US
DecisionSubstantially Equivalent, Jun 23, 1989
ReceivedMay 15, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893669

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.