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: QNQ FDA class 2

Low Dead Space Piston Syringe

General Hospital

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The Low Dead Space Piston Syringe is a medical device designed to reduce medication waste by minimizing the residual volume remaining in the syringe after injection, consisting of a calibrated hollow barrel, a moveable plunger, and optionally a needle. It may be used by healthcare professionals or for patient self-injection. This device is classified as FDA Class 2, requiring 510(k) clearance, under regulation 880.5860 in the General Hospital specialty. It carries product code QNQ and is not an implant and not life-sustaining.

510(k) Clearances

10 matches
K Number
Device Name
Small Volume 0.2mL Syringe
SOL-M Luer Lock Syringe (Low Dead Space) w/o Needle, SOL-M Slip Tip Syringe (Low Dead Space) w/o needle, SOL-M Luer Lock Syringe (Low Dead Space) w/Exchangeable Needle, SOL-CARE Luer Lock Syringe (Low Dead Space) w/Safety Needle, SOL-M Slip Tip Syringe (Low Dead Space) w/Exchangeable Needle
Hypodermic Needle-Pro® EDGE™ Safety Device with Low Dead Space Syringe
PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe
TopFine® LDS (Low Dead Space) Syringe (2 models (TS-LDS2334, TS-LDS2534))
PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe, PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe
FEELject LDV (Low dead volume) syringe
Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe
LDV((Low Dead Volume )Syringe
PLPT LDV (Low Dead Volume) Sterile Syringe

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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