ClearanceBrief
510(k) K100626 ยท KNG Monitor, Ultrasonic, Fetal

DOPPLER FETAL HEART RATE DETECTOR, MODEL FM-200

ApplicantShenzhen Biocare Electronics Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, May 21, 2010
ReceivedMar 5, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100626

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.