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: BTI FDA class 2

Compressor, Air, Portable

Anesthesiology

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The Compressor, Air, Portable is a portable powered device that compresses ambient air for delivery to patients or medical equipment in clinical settings, commonly used to power pneumatically driven medical devices. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is BTI, regulated under 21 CFR 868.6250 in the Anesthesiology specialty.

510(k) Clearances

50+ matches
K Number
Device Name
OMBRA TABLE TOP COMPRESSOR
MEDICAL AIR COMPRESSOR
DK50 DS
EMG TRITON -COMP,MODEL NCA01-XXX SERIES
MEDICAL COMPRESSOR, MODELS DK50 D AND DM
MINIMATE COMPRESSOR
VENTILAIR II MEDICAL AIR COMPRESSOR
NEWPORT C250 AIR COMPRESSOR MODEL C250
MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER
MEDICAL AIR COMPRESSOR
AEROMIST LT, MODEL HCS15004
VIGORMIST COMPRESSOR NEBULIZER
COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81E
PULMO-MIST COMPRESSOR MODEL # 4323
MISTER NEB NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS123
PRONEB ULTRA MODEL NUMBER 85B0100
SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050
MEDICAL AIR COMPRESSOR, MODEL # 8413419
DEVILBISS 8650D
ALRECO 40400
AM-50 AEROSOL/MEDICATION AIR COMPRESSOR
MICROTIME
MODEL #5000 PULMO PLUS
503 MAXI COMPRESSOR
PM PUMP COMPRESSOR
NEBULIZER PUMP, POWERED, MODEL 1110
NEBULIZER PUMP, POWERED MODEL 1180
DEVILBISS MODEL 4650 COMPRESSOR NEUBULIZER
SAM ST
NEBULIZER SYSTEM
AIR STAR
AIR PLUS NEBULIZER
MAXI ASPIRATOR
#504 MINI COMPRESSOR
PM14 SOFT AIR COMPRESSOR
MAXI COMPRESSORS
PORTABLE AIR COMPRESSOR MODEL NUMBER 8125
TURBO AIR COMPRESSOR 8000
LUMINEB I
MULTIICHALLENGE NEBULIZER SYSTEM
NEBULIZER PUMP POWERED MODELS 020 AND 050
ECONO-MIST PORTABLE COMPRESSOR DRIVEN NEBULIZER
SIEMENS DRY AIR COMPRESSOR
AEROSOL ONE, NEBULIZER PUMP
BIRD 6500 AIR COMPRESSOR
MOBIL 02
DURA NEB(TM) 2000 PORTABLE COMPRESSOR
BUNN MODEL 510 MEDICATION COMPRESSOR
ERIE-NEB
AEROSOL ONE

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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