ClearanceBrief
510(k) K881605 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

BIOPSY GUIDE

ApplicantTeknar, Inc., Fenton MO, US
DecisionSubstantially Equivalent, Jun 21, 1988
ReceivedMar 29, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881605

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.