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: FMH FDA class 1

Container, Specimen, Sterile

Pathology

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The Sterile Specimen Container is a sealed, sterile receptacle used to collect and transport biological specimens such as urine, tissue, or other bodily fluids for laboratory analysis without contamination. It is classified as FDA Class 1 (lowest risk) and is subject only to general controls. The product code is FMH, regulated under 21 CFR 864.3250 in the Pathology specialty.

510(k) Clearances

23 matches
K Number
Device Name
TRI-TECH URINE SPECIMEN KIT
VARIOUS-SPECIMEN COLLECTORS
CALCULI FILTER CUP
LANCER SPECIMEN CONTAINER
SPECIMEN SET
URINE SPECIMEN CONTAINER #'S 1013-1016
MIDSTREAM COLLECTION KIT
ABCO MIDSTREAM URINE COLLECTION SET
SPECIMEN COLLECTION PAN
PARA-PAK CLEAN VIAL
LANCER SPECIMEN CONTAINER
SPECIMAN CUP & EMESIS BASIN
JUHN TYM-TAP
OPERATING ROOM SPECIMEN CONTAINER
24-HOUR URINE COLLECTION COOLING WRAP
URINE SAMPLE COLLECTION KIT
CATH KIT, URINE SPECIMEN
SPECIMEN COLLECTION DEVICE
UNICATCH
MID-STREAM COLLECTION SET
SPECIMEN COLLECTOR
4 1/2 OZ. GRADUATED SPECIMEN CONTAINER
CUP, DISPOSABLE SPECIMEN

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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