ClearanceBrief
510(k) K090912 ยท ITX Transducer, Ultrasonic, Diagnostic

DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, MODEL DP-6900

ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd., Nanshan, Shenzhen, CN
DecisionSubstantially Equivalent, Apr 15, 2009
ReceivedApr 1, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090912

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.