ClearanceBrief
510(k) K890173 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

INTERSPEC APOGEE

ApplicantInterspec, Inc., Conshohocken PA, US
DecisionSubstantially Equivalent, Apr 14, 1989
ReceivedJan 17, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890173

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.