ClearanceBrief
510(k) K993342 ยท KNW Instrument, Biopsy

DUCPREP BREAST ASPIRATOR, MODEL PMPO2

ApplicantWindy Hill Technology, Inc., Menlo Park CA, US
DecisionSubstantially Equivalent, Dec 23, 1999
ReceivedOct 5, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993342

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.