ClearanceBrief
510(k) K896999 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

SDL 310 DIAGNOSTIC ULTRASOUND INSTRUMENT

ApplicantShimadzu Corp., Gardena CA, US
DecisionSubstantially Equivalent, Aug 9, 1990
ReceivedDec 13, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896999

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.