ClearanceBrief
510(k) K984446 ยท KXK Source, Brachytherapy, Radionuclide

`BI I-125 BRACHYTHERAPHY SEED, MODEL 125SL & 125SH

ApplicantUrocor, Inc., Oklahoma City OK, US
DecisionSubstantially Equivalent, Apr 16, 1999
ReceivedDec 14, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984446

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.