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: EMX FDA class 1

Balloon, Epistaxis

Ear, Nose, Throat

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The epistaxis balloon is an inflatable device inserted into the nasal cavity to apply pressure and control nosebleeds that cannot be managed by conventional methods. It is classified as FDA Class 1, meaning it poses the lowest risk and is subject only to general controls. The product code is EMX, regulated under 21 CFR 874.4100 in the Ear, Nose, Throat specialty. No special regulatory flags apply to this device.

510(k) Clearances

47 matches
K Number
Device Name
PosiSep X BAM Hemostat Dressing/Intranasal Splint
NASALCEASE
RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERIOR 100MM, MODEL RR-P 100
HYLASINE
HYDROFERA BACTERISTATIC NASAL DRESSING
MEROGEL NASAL DRESSING AND SINUS STENT
ENTAXIS NASAL PACKING
NOSEBLEED NOSECLIP
ULTRACELL PACKING WITH SLEEVE
DISPOSABLE SILICONE EPISTAXIS CATHETER
VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPISTAXIS CATHETER KIT V-2703K
RHINOCELL NASAL PACKINGS
POST-STOP EPISTAXIS CATHETER
EPI-STOP EPISTAXIS CATHETER
EPI-MAX EPISTAXIS CATHETER
DISPOSABLE SILICONE EPISTAXIS CATHETER V-27030/DISPOSABLE SILICONE EPISTAXIS CATHETER KIT V-27030K
EPISTAXIS NASAL PACK
IVALON NASAL PACKING W/DRAWSTRING (8.0CM & 4.5CM), IVALON NASAL PACKING W/AIRWAY TUBE & DRAWSTRING, IVALON CONTOUR NASAL
RAND NASAL PACKING
EXPANDACELL INJECTO-PAK
EXPANDACELL INJECTO-PAK NASAL PACK
EXPANDACELL ANATOMICAL POSTERIOR NASAL PACK W/& WITHOUT AIRWAY
EXPANDACELL INJECTO-PAK NASAL PACK
HYDROCELL NASAL AND SINUS PACKS
EPISTAXIS BALLOON CATHETER WITH PACKING
EXPANDACELL NASAL PACK WITH AIRWAY
ANTERIOR/POSTERIOR EPISTAXIS CATHETER
EPISTAT-II NASAL CATHETER
FLUOROFILM(R)
THE EXPANDACELL SINUS PACK
INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA
MEROCEL EPISTACIS KIT
NASAL-SINUS PACKING
ULTRACELL NASAL PACKING
EPISTAXIS NASAL BALLOON CATHETER
EXPANDACEL NASAL TAMPONS, MODIFICATION
EXPANDACEL NASAL TAMPONS
MODIFIED BIVONA EPISTAXIS CATHETER
EXPANDACEL NASAL TAMPONS
ULTRASTAT NASAL CATHETER
INNOVATIONS NASAL TAMPON
FOX POST NASAL BALLOON CATHETER
EPISTAXIS CATHETER/KIT
GOTTSCHALK NASOSTAT SLIM LINE, ADULT/SM.
NASOSTAT
NASOSTAT
ECHO-OIL

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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