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: BXK FDA class 1

Gas, Calibration (Specified Concentration)

Anesthesiology

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The Gas, Calibration (Specified Concentration) is a gas mixture of precisely known composition used to calibrate medical gas analyzers and monitoring instruments, ensuring measurement accuracy in clinical and laboratory settings. It is classified as FDA Class 1, the lowest risk category, subject to general controls only with no premarket submission required. The product code is BXK, regulated under 21 CFR 868.6400 in the Anesthesiology specialty.

510(k) Clearances

32 matches
K Number
Device Name
BLOOD GAS MIXTURES
LUNG DIFFUSION MIXTURES
LUNG DIFFUSION MIXTURE
MEDICAL MIXTURE-LUNG DIFFUSION GAS MIXTURES
MED-TECH LUNG DIFFUSION MIXTURE
MEDICAL MIXTURE-CLINICAL BLOOD GAS MIXTURES
CALIBRATION GAS
CLINICAL BLOOD GAS MIXTURE
CLINICAL BLOOD GAS MIXTURE
BLOOD GAS MIXTURE
CLINICAL BLOOD GAS
CALIBRATION GAS
BLOOD GAS MIXTURE
LUNG DIFFUSION GAS MIXTURE
CALIBRATION KIT
LUNG DIFFUSION GAS MIXTURES
ANESTHETIC GAS CALIBRATION MIXTURE
MEDIBLEND (TM) LUNG DIFFUSION GAS MIXTURES
LUNG DIFFUSION GAS
CALIBRATION GAS FOR CARBON DIOXIDE MONITOR
BLOOD ANALYSIS GAS
O.1 TO 25.0% CARB. DIOX. U.S.P. BALANCE OXYGEN USP
O.1 TO 50.0% CARBON DIOXIDE, USP BALANCE NITRO.,NF
O.1 T0 40.0% CARBON DIOX. O.1 TO 90.0% OXY. U.S.P
0.1 TO 25.0% OXYGEN, USP, BALANCE NITROGEN, N.F.
GAS, CALIBRATION, SPECIFIED CONCENTRATION
CALIBRATION GAS FOR SERVO GAS MONITOR 120
ANAEROBIC CARBON DIOXIDE
CLINICAL GAS MIXTURE-NON-FLAMMABLE
BLOOD GAS MIXTURE
LUNG DIFFUSION MIXTURE
CLINICAL GAS MIXTURE-FLAMMABLE

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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