ClearanceBrief
510(k) K890203 ยท FCG Biopsy Needle

ADMS BIOPSY NEEDLE

ApplicantAdvanced Diagnostic Medical Systems, Inc., Dublin CA, US
DecisionSubstantially Equivalent, Mar 8, 1989
ReceivedJan 17, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890203

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.