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: JJM FDA class 1

Osmometer For Clinical Use

Clinical Chemistry

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This device is an osmometer for clinical use that measures the osmolality of biological fluids such as serum and urine, providing information used in the assessment of fluid and electrolyte balance, renal concentrating ability, and toxic alcohol ingestion. It is classified as FDA Class 1, indicating low risk and requiring only general controls without a premarket notification. The product code is JJM, regulated under 21 CFR 862.2730, within the Clinical Chemistry medical specialty.

510(k) Clearances

12 matches
K Number
Device Name
THE ADVANCED OSMOMETER (3900)
ADVANCED MICRO-OSMOMETER MODEL 3300
MODEL 3D3 OSMOMETER
OSMOMETER MODEL 2400
OSMOMETER MODEL 110
AO-10 AUTOMATED OSMOMETER
OSMOTIC PRESSURE AUTO & STAT OM-6010
WESCOR 5500 VAPOR PRESSURE OSMOMETER
COLLOID OSMOMETER 4400
MICRO-SAMPLE OSMOMETER 3M0
OSMOMETER MODEL OM-6010
OSMOMETER MODEL 3W11

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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