ClearanceBrief
510(k) K223387 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System

ApplicantSamsung Medison Co., Ltd., Hongcheon-Gun, KR
DecisionSubstantially Equivalent, Feb 13, 2023
ReceivedNov 7, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223387

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.