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: ILP FDA class 1

System, Communication, Non-Powered

Physical Medicine

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A Non-Powered Communication System is a low-technology augmentative and alternative communication device used in Physical Medicine and occupational therapy to assist patients with speech or motor impairments in communicating, typically consisting of symbol boards, letter charts, or picture-based communication aids that require no electrical power. It is classified as FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. The product code is ILP, regulated under 21 CFR 890.3700, within the Physical Medicine medical specialty. This device is GMP exempt, indicating it is not subject to full good manufacturing practice requirements.

510(k) Clearances

21 matches
K Number
Device Name
TELL ME TAGS - NONPOWERED COMMUNICATION SYS
SPEECH TEACHER
ADAPTIVE PENS & LAP DESK
MOUTH STICK KIT
HOLDER FOR MOUTH STICK
ADJ. WOODEN BOARD FOR WRITING
PICTURES & WORD IDENTIFICATION CVA PAT
BK-4015 ECONOMY COMMUNICATION SHEET
KIT OF WORDS & LTRS TO RE-LEARN-BK4014
FLEXIBLE HOLDER TO HOLD PHONE RECEIVER
PLASTIC STOP TO HOLD TELEPHONE BUTTON
PLASTIC SLIP-ON POINTS W/RUBBER TIP FOR
PLASTIC SLIP-ON PEN/PENCIL HOLDER
TELEPHONE ADAPTOR-PERSONS CANT ANSWER
VACUUM WAND AND UNI-READER
STIM STAND
BOOK HOLDER
NON-POWERED COMMUNICATION SYSTEMS
BOOK HOLDER
PAGE TURNER
KEYBOARD SHEILDS

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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