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: PMN FDA class 2

Assayed External Control Material For Microbiology Nucleic Acid Amplification (Nat) Assays

Microbiology

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The Assayed External Control Material For Microbiology Nucleic Acid Amplification (NAT) Assays (product code PMN) is a Class 2 microbiology device consisting of assayed external quality control material used to monitor the performance of microbiology nucleic acid assays for in vitro diagnostic use, regulated under 866.3920. It requires 510(k) clearance. The device is not an implant and is not life-sustaining.

510(k) Clearances

26 matches
K Number
Device Name
SPOTFIRE RSP Pos & Neg Controls; SPOTFIRE RSP Negative Control
SPOTFIRE RSP Pos & Neg Controls (M425), SPOTFIRE RSP Positive Control (M42638), SPOTFIRE RSP Negative Control (M42738)
MDx-Chex for BC-GN
MDx-Chex for BC-GP
SPOTFIRE® RSP Pos & Neg Controls, SPOTFIRE® RSP Positive Control, SPOTFIRE® RSP Negative Control
SPOTFIRE RSP Positive Control, SPOTFIRE RSP Negative Control
BioFire JI Control Panel M420
NATtrol BD MAX Vaginal Panel External Controls
MDx-Chex for BCID2
BioFire RP2.1/RP2.1plus Control Panel M441
FilmArray Global Fever Panel External Control Kit
FilmArray BCID2 Control Panel M416
Cepheid Xpert Respiratory Control Panel
Cepheid Xpert SA Nasal Complete Control Panel
Cepheid Xpert MRSA NxG Control Panel
Cepheid Xpert CT/NG Control Panel
FilmArray Pneumonia/Pneumoniaplus Control
Cepheid Xpert C. difficile/Epi Control Panel
Cepheid Xpert GBS LB Control Panel
BD MAX CT/GC/TV 20-Day QC Panel
BD MAX Enteric Parasite Control Panel, BD MAX Enteric Parasite 20-Day QC Panel
FilmArray RP2/RP2plus Control Panel
FilmArray Warrior Control Panel M290
FilmArray RP EZ Control Panel M265
Amplichek I, Negative , Amplichek I, Level 1, Amplichek I, Level 2, Amplichek I, Level 3, Amplichek I, MiniPak
Amplichek II, Negative and Amplichek II, Negative MiniPak, Amplichek II, Level 1 and Amplichek II, Level 1 MiniPak, Amplichek II, Level 2 and Amplichek II, Level 2 MiniPak, Amplichek II, Level 3 and Amplichek II, Level 3 MiniPak

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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