Cleared Traditional

Lumify Diagnostic Ultrasound System (K242519) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K242519 · Philips Ultrasound · Radiology device
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May 2025
Decision
265d
Days
Class 2
Risk

K242519 is an FDA 510(k) clearance for the Lumify Diagnostic Ultrasound System. Classified as System, Imaging, Pulsed Doppler, Ultrasonic within the IYN classification (a category covering pulsed Doppler and ultrasound imaging systems), Class II - Special Controls.

Submitted by Philips Ultrasound (Bothell, US). The FDA issued a Cleared decision on May 15, 2025 after a review of 265 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1550 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Philips Ultrasound devices

Submission Details

510(k) Number K242519 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 23, 2024
Decision Date May 15, 2025
Days to Decision 265 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
158d slower than avg
Panel avg: 107d · This submission: 265d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IYN System, Imaging, Pulsed Doppler, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1550
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - IYN System, Imaging, Pulsed Doppler, Ultrasonic

All 632
Devices cleared under the same product code (IYN) and FDA review panel - the closest regulatory comparables to K242519.
Diagnostic Ultrasound System (Recho R9W)
K250020 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · May 2025
6450 Ultrasound System (MyLabE80)
K241671 · Esaote, S.P.A. · May 2025
Diagnostic Ultrasound System (MX6)
K250110 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · May 2025
Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V8.5
K242808 · Canon Medical Systems Corporation · May 2025
EPIQ Series Diagnostic Ultrasound Systems
K251110 · Philips Ultrasound, LLC · May 2025
Lumify Diagnostic Ultrasound System
K242670 · Philips Ultrasound · May 2025