ClearanceBrief
510(k) K060410 ยท HEK Monitor, Heart Sound, Fetal, Ultrasonic

ECHOHEART TRANSVAGINAL DOPPLER PROBE

ApplicantSummit Doppler Systems, Inc., Golden CO, US
DecisionSubstantially Equivalent, Apr 10, 2006
ReceivedFeb 16, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060410

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.