ClearanceBrief
510(k) K243702 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System

ApplicantSamsung Medison Co., Ltd., Hongcheon-Gun, KR
DecisionSubstantially Equivalent, Feb 12, 2025
ReceivedNov 29, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243702

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.