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: ITI FDA class 2

Wheelchair, Powered

Physical Medicine

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A powered wheelchair is an electrically driven mobility device for individuals who cannot self-propel a manual wheelchair due to physical limitations, providing independent powered mobility control via joystick or other input. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is ITI, regulated under 21 CFR 890.3860, within the Physical Medicine medical specialty. This device is eligible for third party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Power Wheelchair (MOB1107)
Electric Wheelchair (HG-630)
Power Wheelchair (D26)
ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02)
Electric Wheelchair (BC-EA5516, BC-EC8002, BC-EC8003, BC-EALD3)
Electric Wheelchair (F309)
eFOLDi Navigator Powerchair (STPC-A)
Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003)
KLAXON (TWIST); KLAXON (TWIST R)
Electric Wheelchair (LW01301A07)
Powered wheelchair (mobility robot) (M4, M4U)
Power Wheelchair (YH-E6011,YH-E6013A)
Electrically powered wheelchair
Portable Wheelchair
Handbike Batec Electric
Electrically Powered Wheelchair
Electrically Powered Wheelchair
Electric Wheelchair (YE200)
Klaxon (Twist); Klaxon (Twist R)
Power Wheelchair (D03, D05, D06, D09, D11, D16, D22, D23, D26, D36)
Power Wheelchair (D10, D12, D15, D17, D20, D37)
Electric Wheelchair (MODEL H)
Power Wheelchair
Electric Wheelchair (HC820N)
Empulse M90
Power wheelchair
Electric Wheelchair (KR8803)
Powered Wheelchair (NXN20-209)
Powered Wheelchair (NXN20-208, NXN20-211)
Power Wheelchair (W5538)
Power wheelchair
Power-Flex (PFX1214); Power-Flex (PFX1517); Power-Flex (PFX1820)
Electric wheelchair (KR-8807)
Electric Wheelchair (ME23-EW16-BC200-01); Electric Wheelchair (ME23-EW16-BC200-02)
Electrically powered wheelchair (HP202)
Electrically powered wheelchair
Power Wheelchair (JJW-6001)
Power Wheelchair
Electric wheelchair (YHWL002, YHWL003)
Power Wheelchair (YH-E7007)
Powered Wheelchair (NXN20-205, NXN20-205M)
Electric wheelchair (C001)
Electric wheelchair (W3902)
Electric wheelchair (N3901)
Navigator (FMNVG15); Navigator XL (FMNVX06)
Electric wheelchair (S7018)
Power wheelchair (N6101)
Electric Wheelchair (Panda 10); Electric Wheelchair (Panda 12)
Electric Wheelchair (JLE-W01A-2023)
Electric Wheelchair (Robooter E60) (BBR-E60-01); Electric Wheelchair (Robooter E60) (BBR-E60-02); Electric Wheelchair (Robooter E60) (BBR-E60-03); Electric Wheelchair (Robooter E60) (BBR-E60-04); Electric Wheelchair (Robooter E60) (BBR-E60-05); Electric Wheelchair (Robooter E60) (BBR-E60-06); Electric Wheelchair (Robooter E60) (BBR-E60-07); Electric Wheelchair (Robooter E60) (BBR-E60-08)

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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