ClearanceBrief
510(k) K954999 ยท KNW Instrument, Biopsy

LILY MULTICANNULA GUIDE

ApplicantLily Imaging Solutions Co., Fortuna CA, US
DecisionSubstantially Equivalent, Apr 4, 1996
ReceivedNov 1, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954999

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.