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: MUD FDA class 2

Oximeter, Tissue Saturation

Cardiovascular

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A Tissue Saturation Oximeter is a non-invasive or minimally invasive monitoring device that measures regional oxygen saturation of tissue (rSO2) using near-infrared spectroscopy, providing real-time assessment of tissue oxygenation in organs such as the brain or muscles during surgery or critical care. It is FDA Class 2, requiring 510(k) clearance, with product code MUD under 21 CFR 870.2700 in the Cardiovascular specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

50+ matches
K Number
Device Name
Lap.Ox™ Laparoscopic Tissue Oximeter
Cerebral Autoregulation Index (CAI) Algorithm
ODI-Tech
SnapshotNIR model KD205
OxiplexTS200
Intra.Ox™ 2.0 Handheld Tissue Oximeter
Edwards Algorithm for Measurement of Blood Hemoglobin
Cerebral Adaptive Index (CAI) Algorithm
Masimo O3 Regional Oximeter System
Intra.Ox 2.0 Handheld Tissue Oximeter
INVOS PM7100 Patient Monitor, INVOS Pediatric rSO2 Sensor, INVOS Infant Regional Saturation Sensor (also referred to as OxyAlert NIRSensor)
FORE-SIGHT ELITE Absolute Tissue Oximeter
SnapshotNIR
Masimo O3 Regional Oximeter System
MIMOSA Imager
FORE-SIGHT ELITE Tissue Oximeter Module
T-Stat 2.0 Microvascular Tissue Oximeter
Intra.Ox 2.0 Handheld Tissue Oximeter
Masimo O3 Regional Oximeter System
SenSmart Model 8006CA Reusable Regional Oximetry Sensor, SenSmart Model 8006PI Disposable Patient Interface
INVOS PM7100 Patient Monitor, INVOS Adult rSO2 Sensor
Presygen/si-1
Clarifi Imaging System
FORE-SIGHT ELITE Module Tissue Oximeter
Intra.Ox Handheld Tissue Oximeter
Masimo O3 Regional Oximeter System
Kent Camera
Ox-Imager CS
HyperView Hyperspectral Tissue Oxygenation Measurement System
NIRO-200NX DP
Masimo O3 Regional Oximeter System
SenSmart Model 8203CA Regional Oximetry Sensor (Adult/Pediatric, >40 kg, SenSmart Model 820CA Regional Oximetry Sensor (Adult/Pediatric, >40 kg)
NIRO-200NX
FORE-SIGHT Elite Absolute Tissue Oximeter
INTRA. OX HANDHELD TISSUE OXIMETER
MULTI-PARAMETER MOBILE CAREGUIDE 4100 OXIMETER
ODISSEY TISSUE OXIMETER
FORE-SIGHT ELITE ABSOLUTE TISSUE OXIMETER
MULTI-PARAMETER MOBILE CAREGUIDE 3100 OXIMETER WITH TABLET
MULTI-PARAMETER MOBILE CAREGUIDE 3100 OXIMETER
FORE-SIGHT ELITE ABSOLUTE TISSUE OXIMETER
MOBILE CAREGUIDE 2100 OXIMETER
NOORVMS-OXY TISSUE OXYGEN AND TEMPERTURE MONITOR
KENT CAMERA
CAREGUIDE OXIMETER
MODEL 7600 REGIONAL OXIMETER SYSTEM WITH EQUANOX TECHNOLOGY
FORE-SIGHT ABSOLUTE TISSUE OXIMETER
INPECTRA STO2 SPOT CHECK
CEROX, MODEL 321OF
FORE-SIGHT ABSOLUTE CEREBRAL AND SOMATIC OXIMETER, MC 2000 SERIES, MODELS MC2000, MC2010, MC2020, MC2030

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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