ClearanceBrief
510(k) K091680 ยท ITX Transducer, Ultrasonic, Diagnostic

DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM

ApplicantEdan Instruments, Inc., Yonkers NY, US
DecisionSubstantially Equivalent, Jun 19, 2009
ReceivedJun 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091680

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.