ClearanceBrief
510(k) K082480 ยท KNG Monitor, Ultrasonic, Fetal

CONTEC POCKET FETAL DOPPLER

ApplicantContec Medical System Co., Ltd., Zhong Shan, Shanghai, CN
DecisionSubstantially Equivalent, Feb 25, 2009
ReceivedAug 28, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082480

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.