ClearanceBrief
510(k) K242444 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

HERA W10 Diagnostic Ultrasound System; HERA W9 Diagnostic Ultrasound System

ApplicantSamsung Medison Co., Ltd., Hongcheon-Gun, KR
DecisionSubstantially Equivalent, Nov 27, 2024
ReceivedAug 16, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242444

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.