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: FQM FDA class 1

Bandage, Elastic

General Hospital

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An elastic bandage is a stretchable fabric wrap used to apply compression or support to injured or post-operative body parts, aiding in the management of swelling, sprains, and wound care. It is classified as FDA Class 1 (lowest risk), subject only to general controls, with no premarket submission required. The product code is FQM, regulated under 21 CFR 880.5075, within the General Hospital medical specialty. This device is exempt from GMP requirements.

510(k) Clearances

42 matches
K Number
Device Name
PETIT SILMA ELASTIC BANDAGE WITH GERMANIUM/TITANIUM OXIDE
BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE
COMFORTCARE COMPRESSION SUPPORT WITIH MAGNETS AND AEGIS MICROBE SHIELD COMFORTCARE MAGNETIC INSOLES AND AEGIS MICROBE
SKIN SAVER SYSTEMS
ASPEN ESMARK BANDAGE
TUBE-BANDAGE FOR HUMAN DIGITS 200
MEDICALEX
ORTHO WRAP
COMPRESSOGRIP TUBULAR ELASTIC BANDAGE
TUBULAR STOCKINETTE
BIAS STOCKINETTE
ELASTIC BANDAGE
STRUVA & MEDI
SOF-BAND HIGH STRETCH BANDAGES
ELASTIC GAUZE
ROLL STRETCH GAUZE
ELASTIC BANDAGE
ELASTIC OPEN WEAVE BANDAGE
TUBULAR BANDAGE
ELASTIC BANDAGE CAT.#182-186 (WIDTH)
FINGER PAINGUARD CAT.#193-194
WINTER HEAD DRESSING
STOCKINETTE, STERILE TWO PLY W/PULL TABS
MEDSPEC RUBBER ELASTIC BANDAGES
ANAGO DISP., ALL PURPOSE PATIENT REST.
TOMMY TOES
POROUS ELASTIC RUBBER BANDAGE
BINDAFIX
SECUTEX SURGICAL BINDER
STOCKINETTE, TUBULAR UNBLEACHED
TAPE, ELASTOPLAST ELASTIC TEAR
BANDAGE
TUBULAR DRESSING RETAINER
BANDAGE, ELASTIC
ELASTOMULL GAUZE BANDAGE
CONFORM ELASTIC NETTING
BANDAGE, UNIPRESS, CLARION
BANDAGE, CONFO-LASTIC ALL COTTON ELASTIC
BANDAGE, RAPIDO-LASTIC COTTON/NYLON
BANDAGE, E-COTTON ELASTIC
BANDAGE, WRINKY-LASTIC ELASTIC GAUZE
BANDAGE, CEB COTTON ELASTIC

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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