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: PND FDA class 2

Midline Catheter

General Hospital

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The Midline Catheter (product code PND) is a Class 2 general hospital device that is inserted into the peripheral vascular system for infusion of fluids and medications for less than 28 days, regulated under 880.5200. It requires 510(k) clearance and falls within the general hospital medical specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

13 matches
K Number
Device Name
Midline Catheter
Arrow Pressure Injectable Midline Catheter
Provena(TM) Midline Catheter
Stiletto Extended Dwell Catheter
primeMidline Catheters
Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter
primeMidline Catheters
ArchFlo CT Midline
CT Midline
PowerGlide ST Midline Catheter
PowerMidline Catheter
ARROW Pressure Injectable Midline Catheter with Chlorag+ard Antimicrobial and Antithrombogenic Technology
PowerMidline Catheter

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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