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: GTQ FDA class 1

Antistreptolysin - Titer/Streptolysin O Reagent

Microbiology

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The Antistreptolysin-Titer/Streptolysin O Reagent is a laboratory reagent used to measure antistreptolysin O (ASO) antibody titers in patient serum, serving as an indicator of past or present streptococcal infection and aiding in the diagnosis of conditions such as rheumatic fever and post-streptococcal glomerulonephritis. It is an FDA Class 1 device subject only to general controls, with no premarket clearance required. The product code is GTQ, regulated under 21 CFR 866.3720 in the Microbiology specialty. No special flags apply to this device.

510(k) Clearances

37 matches
K Number
Device Name
VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 28, REF 680 2323; VITROS CHEMISTRY PRODUCTS FS CALIBRATOR 1, REF 6801873;
OLYMPUS ANTI-STERPTOLYSIN O IMMUNOTURBIDIMETRIC REAGENT
TURBIQUANT ASL
BECKMAN ANTI-STREPTOLYSIN O KIT
ACCUTEX ASO LATEX TEST
TECH SIMPLE ANTISTREPTOLYSIN O ASO SERUM CONTROL
BECKMAN ANTISTREPTOLYSIN O, MODIFICATION
BECKMAN ANTI-STREPTOLYSIN O (ASO) KIT
CROATEST (R) RHEUMATOID DIAGNOSTIC
QM300 CALIBRATOR G PACK
QM300 CONTROL G PACK
QM300 ANTISTREPTOLYSIN O (ASO) ANTIGEN PACK
TARGET ASO TEST
RAPITEX(R) ASL NEW
RHEUMAGEN ASO T-CONTROL
ASO-CUBE(TM)
QUANTEX ASO PLUS (LATEX,BUFFER STANDARD,CONTROL)
IMMUNO/ASO
QUIK-DOT ANTISTREPTOLYSIN-O
ASO SLIDE TEST
RAPID AS LATEX
REUMAGEN ASL
LASER ASO KIT
V-TREND ASO PLUS LATEX TEST
ASO SLIDE EIKEN
FISHER DIAGNOSTIC LATEST ASO TEST KIT
SERIMM SURE ASO-CHEK CONTROL SERUM
AS LATEX PLUS
ASO-CHECK
TESTCORP ASO
ASO SURE PLUS
ASO SURE
BI-ASO SLIDE TEST
ASO QUANTUM, ANTISTREPTOLYSIN O TEST
RAPI/TEX ASO STANDARD SERUM
ANTISTREPTOLYSIN (ASO) LATEX SLIDE TEST
REAGENT, LYOPHILIZED ANTI-STREPTOLYSIN O

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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