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: FYD FDA class 2

Apparatus, Exhaust, Surgical

General, Plastic Surgery

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A surgical exhaust apparatus is a ventilation device used in operating rooms to remove contaminated air, particulate matter, aerosols, or anesthetic gases from the immediate surgical environment, improving air quality and infection control. It is classified as FDA Class 2 (moderate risk), subject to general and special controls, and requires 510(k) premarket notification. The product code is FYD, regulated under 21 CFR 878.5070, within the General, Plastic Surgery medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
PlumeSafe X5 Smoke Management System
8Q10 Surclear Smoke Plume Evacuation System
Medline Smoke Evacuation Shroud
NEBULAE SRS Laparoscopic Surgical Smoke Removal System
Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF Sensor
EvaQMax Smoke Evacuation System
Megadyne Foot Switch
SafeAir Smoke Evacuator compact
Smoklean
Crystal Vision
RapidVac Smoke Evacuator System
VISICLEAR SMOKE EVACUATION SYSTEM
CONMED AER DEFENSE SMOKE EVACUATOR
SERVICE MANAGER SM40SE
LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM
MASTEL LASER CLEAN ROOM, MODEL EBS-100
LAFACI
SMOKE EVACUATION HOSES/TUBING
NEPTUNE WASTE MANAGEMENT STSTEM
CRYSTAL VISION #250D SMOKE EVACUATOR SYSTEM WITH ACCESSORIES
STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100
PENADAPT 10
NEPTUNE WASTE MANAGEMENT SYSTEM
PALL SURGICLEAR LAPAROSCOPIC SMOKE FILTRATION SYSTEM, MODEL CLSF1
BUFFALO FILTER VIROSAFE ERBIUM:YAG FILTER - #VSEYAG1-4 BUFFALO FILTER VIROSAFE ERBIUM:YAG PREFILTER - #BFEYAG04PF
BUFFALO FILTER VIROSAFE HRF- #VSHRFO1
BUFFALO FILTER VIROSAFE 18 FILTER-CATALOG #VSO1801
STERIS SMOKE EVACUATION SYSTEM
VALLEYLAB OPTIMUMM SMOKE EVACUATOR SYSTEM
SKYVAL
SMARTVAC SMOKE EVACUATION SYSTEM
FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC
BUFFALO FILTER REPLACEMENT FILTER #BSPF030
BUFFALO FILTER REPLACEMENT FILTER #BSUCF03
BEI MEDICAL SYSTEMS' SMOKE EVACUATOR
SNJ SMOKE EVACUATION SUCTION WAND
CRYSTAL VISION AND ACCESSORIES
ACU-EVAC
BUFFALO FILTER REPLACEMENT FILTER #BST300UL
BUFFALO FILTER REPLACEMENT FILTER #BPTU100
REUSABLE TOWEL AND GOWN PACKS
PLUMEMASTER SMOKE EVACUATION SYSTEM
BUFFALO FILTER REPLACEMENT FILTER #BCULPA
BUFFALO FILTER REPLACEMENT FILTER #BCCHAR
BUFFALO FILTER REPLACEMENT FILTER #BCR0030
BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO
BUFFALO FILTER REPLACEMENT FILTER #BCR0043
VICROSAFE 6 AND VICROSAFE 12
BUFFALO FILTER REPLACEMENT FILTER BST312PF
BUFFALO FILTER REPLACEMENT #BLFS-101/103

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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