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: KLK FDA class 2

Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia

Anesthesiology

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The Cutaneous Oxygen Monitor for Infants Not Under Gas Anesthesia is a non-invasive monitoring device that measures transcutaneous oxygen partial pressure through the skin surface, used to continuously assess oxygenation status in neonatal and pediatric patients. It is classified as FDA Class 2, indicating moderate risk requiring 510(k) premarket clearance. The product code is KLK and it is regulated under 21 CFR 868.2500 in the Anesthesiology specialty.

510(k) Clearances

47 matches
K Number
Device Name
MICROGAS 7650 TRANSCUTANEOUS MONITOR
MICROGAS 7650 TRANSCUTANEOUS MONITOR
SIEMENS SC9000/SC9015 TCP02/C02 MODULE
SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETE
OXYCARE(TM) OXYGEN CONTROLLER/MONITOR
HEWLETT-PACKARD MODEL M1018A TCPO2/TOPCO2 MODULE
HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX
MODEL 840 TRANSCUTAN. OXYGEN/CARBON DIOX. MONITOR
515A NEO-TRAK NEONATAL MONITOR
HORIZON 2000 TRANSCUTANEOUS GAS MONITORING
KONTRON CUTANEOUS PO2 MONITOR 820
PO-510 TCPO2 MONITOR
STAT GAS MODULE
NOVAMETRIX 811 TRANSCO2M PORTABLE TRANSCUTANEOUS 2
NOVAMETRIX 860 PROTA. TRANSCUTANEOUS OXYGEN
SERVOMED OXYMONITO SMK 363
NOVAMETRIX 850 TRANSCUTANEOUS OXYGEN
TRANSCUTANEOUS 800-OXYGEN MONITORS/801
MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT
DAYPAK SYS VII CATHETER CARE KIT
PATIENT MONITOR #404
IL 301 PORTABLE TRANSCUT. OXYGEN MONI
OXY MONITOR 5-RANGE DUAL-THERMISTOR
TRANSCUTANEOUS BLOOD OXYGEN SENSOR SYS
TRANSCUTANEOUS OXYGEN MONITOR OPTION
AS 30/TCP MODULE
IL 301 TRANSCUTANEOUS OXYGEN MONITOR
CRITIKON OXYGEN MONITOR, MODEL 8030
NOVAMETRIX MODEL 807 TRANSCUT. MONITOR
CRITIKON TRANSCUTANEOUS GAS MONITORS
NOVAMETRIX MODEL 816A TRANSCUT. OXYGEN
NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER
MODEL 78850 OXYGEN MONITOR
PO-200 BLOOD OXYGEN MONITOR
CORDIS TCPO2 TRANCUTANEOUS OXYGEN PRESS
LIFESPAN 100
TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300
TCM202 TCPO2 & TCM204 TCPO2/PO2 REC. SY.
NOVAMETRIX TCOMETTE #809 TRANS. MONITOR
OXYMETER
ROCHE SENSOR ADAPTOR
TC02M PRECISION GAS CALIBRATOR
TC02M ELECTRODE ADHESIVE RINGS
TC02 M OXYGEN ELECTRODE CONTACT
TCO2M MODEL 818
MONITOR, SENSOMATIII OXYGEN
TRANSCUTANEOUS OXYGEN PERFUSION MONITOR

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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