ClearanceBrief
510(k) K862322 ยท HHT Spatula, Cervical, Cytological

CHLAMYDIA KIT, STD KIT

ApplicantIntl. Cytobrush, Inc., Hollywood FL, US
DecisionSubstantially Equivalent, Jul 7, 1986
ReceivedJun 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862322

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.