ClearanceBrief
510(k) K242670 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

Lumify Diagnostic Ultrasound System

ApplicantPhilips Ultrasound, Bothell WA, US
DecisionSubstantially Equivalent, May 8, 2025
ReceivedSep 5, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242670

DateFirm and productCodeLinked 510(k)
Oct 16, 2026Philips Ultrasound, LLC
Philips Lumify Diagnostic Ultrasound System
Open, Classified
IYNNone listed
Dec 4, 2025Philips Ultrasound, LLC
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Open, Classified
IYNNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.