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: CCL FDA class 2

Analyzer, Gas, Oxygen, Gaseous-Phase

Anesthesiology

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The Gaseous-Phase Oxygen Analyzer is an anesthesiology device that measures the concentration of oxygen in the gas phase of a breathing circuit or inspired gas stream, used to verify that appropriate oxygen concentrations are being delivered to patients during anesthesia, ventilation, or oxygen therapy. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification. The product code is CCL, regulated under 21 CFR 868.1720, within the Anesthesiology medical specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
Smart Check O2 (MA0236)
Maxtec MaxO2 ME+p
Percent Oxygen Sensors
OxyMinder
Accu O2 Oxygen Analyzer
MaxO2ME
CARESCAPE RESPIRATORY MODULES, E-SCO, E-SCOV, E-SCAIOV AND ACCESSORIES
ENVITEC MYSIGN O OXYGEN MEASURING DEVICE
ULTRAMAXO2 OXYGEN ANALYER
ENVITEC MEDICAL OXYGEN SENORS, MODELS OOM101; 00M102/-1;OOM103/-1/-1M;OOM104;OOM105;00M106
DIGIFLO CONCENTRATOR ANALYZER
PRECISION OXYGEN MONITOR
MAXO2 CU
OXYGEN ANALYZER, MODELS AII 20000A, AII 2000HC, AII 2000M
DATEX-OHMEDA S/5 COMPACT AIRWAY MODULE (MODEL FAMILY E-CAIOVX) E-CAIOVX, E-CAIOV, E-CAIO, E-COVX, E-COV, E-CO & ACCESACC
OXYGEN MEDICELS, CITICELS
MAXO2+, MODEL A AND AE
RX300 OXYGEN ANALYZER
MX 300 OXYGEN MONITOR
OXICHECK
PRIMA OXYGEN MONITOR
'ALL 2000' % OXYGEN ANALYZER
100 SERIES OXYGEN ANALYZER, MODELS 1000-E AND 1000-I
M-XX OXYGEN SENSORS
SENSIDYNE OXYGEN ANALYZER & SENSIDYNE OXYGEN MONITOR
OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130
TED 200T7 OXYGEN MONITOR
TED 60T OXYGEN ANALYZER
SIEMENS FIO2 SENSOR
INVACARE CHECK O2 PLUS CONCENTRATOR ANALYZER (CHECK O2 PLUS)
PRO2 CHECK OXYGEN INDICATOR
HP ANESTHESIA GAS MONITOR (WATERTRAP), MODEL A02
MODEL 02 OXYGEN ANALYZER
VACU*MED GOLD EDITION OXYGEN GAS ANALYZER
CERAMATEC MAXCELL AND CAG GALVANIC OXYGEN SENSORS
HANDI OXYGEN ANALYZER
TED 191
VENTREX OXYGEN SENSOR
GASEOUS OXYGEN ANALYZER (MODEL S-3A) MODIFICATION
MINIOX 3000 OXYGEN MONITOR
OXYCHECK OXYGEN MONITOR
PERCENT OXYGEN SENSOR
SEATRONICS FAMILY OF GALVANIC OXYGEN SENSORS
OXYGEN CONCENTRATION STATUS INDICATOR (O.C.S.I.)
FI02 SENSING MODULE
OXYCHEK OXYGEN ANALYZER
OXYGEN CONCENTRATION INDICATOR
MINIOX 1000 OXYGEN CONCENTRATION INDICATOR
PRO2 OXYGEN ANALYZER
VTI OXYGEN ANALYZER

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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