Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: IYO FDA class 2

System, Imaging, Pulsed Echo, Ultrasonic

Radiology

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A pulsed echo ultrasonic imaging system uses reflected sound waves to produce real-time cross-sectional images of internal organs and tissues, widely applied in diagnostic imaging across multiple clinical specialties. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) clearance before commercial distribution. The product code is IYO, regulated under 21 CFR 892.1560, within the Radiology medical specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
B-Scan
Velacur One (LI-1100)
Accuro 3S
EchoGuide (Version 1)
Portable Liver Elastography Ultrasound Diagnostic System (Liverscan C)
SpineUs™ System
Velacur
SC1 Handheld Ultrasound Imaging system (Model: SC1)
ACUSON SC2000 Diagnostic Ultrasound System
B-Ultrasound Diagnostic System
Pocket III
EdgeFlow UH10
BD Prevue™ II Peripheral Vascular Access System
Portable Liver Elastography Ultrasound Diagnostic System (Liverscan Mobile)
Bladder Scanner
Endoscopic Ultrasonic Diagnostic Equipment /Disposable Sterile Endoscopic Ultrasonic Probe (USW-S1,USW140-S20MS)
iSR`obot Mona Lisa 2.0
K3900 Ultrasound Imaging System
Velacur
SiteRite™ 9 Ultrasound System
Bladder Scanner Model: BVT02
Velacur
Butterfly iQ/iQ+ Ultrasound System
FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630)
Sunkingdom Ophthalmic Ultrasound Examination Instrument SK-3000A, SK-3000B, SK-3000C, SK-2000AP, SK-2000A, SK-2000P
QT Scanner 2000 Model A
Bladder Scanner, Model Name:M5
NAVIRFA Scope
ATUSA™ Automated 3D Breast Ultrasound System
EchoSK and EchoSGyn modules for EchoS Family devices
iSR’obot Mona Lisa 2.0
Makoto Intravascular Imaging System, TVC-MC10/TVC-MC10i, Dualpro IVUS + NIRS Imaging Catheter ,TVC-C195-42, Peripheral 014 Imaging Catheter, TVC-E195-42
MD-320W Ultrasound Biomicroscope
Axialis Ophthalmic Ultrasound System
Acuson SC2000 Diagnostic Ultrasound System
FibroScan 230
SC1 Handheld Ultrasound Imaging System (Model: SC1)
iSR'obot Mona Lisa 1.0
BD Prevue II Peripheral Vascular Vascular Access System
THD Procto Software System
Palm Bladder Scanner - PBSV7.1
Breast Volume Navigator (BVN) Model G-2000
FibroScan® Family of Products (Models: 502 Touch, 530 Compact, 430 Mini+, and 630)
Bladder Scanner (Model: M3, M3-HD, M4, M4-HD)
IntraSight Mobile
AcuSee AS-P1000 System
CUBEScan BioCon-1100
Liver Incytes, Model 1005
FibroScan® 630
Auto 3D Bladder Volume Tool

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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