ClearanceBrief
510(k) K925999 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

SWEMED NEEDLE GUIDE

ApplicantSwemed Lab Intl., Chicago IL, US
DecisionSubstantially Equivalent, Oct 3, 1994
ReceivedNov 27, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925999

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.