ClearanceBrief
510(k) K140579 ยท KNG Monitor, Ultrasonic, Fetal

ULTRASONIC POCKET DOPPLER

ApplicantEdan Instruments, Inc., Shenzhen, Guangdong, CN
DecisionSubstantially Equivalent, Feb 6, 2015
ReceivedMar 6, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140579

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.