ClearanceBrief
510(k) K922051 ยท KOD Catheter, Urological

KIT PAK'S FLUSHING KIT

ApplicantKit Pak, Inc., Elk Grove Village IL, US
DecisionUnknown, Jun 17, 1993
ReceivedMay 1, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922051

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.