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: FAP FDA class 2

Cystometric Gas (Carbon-Dioxide) On Hydraulic Device

Gastroenterology, Urology

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The Cystometric Gas (Carbon-Dioxide) or Hydraulic Device (product code FAP) is a urodynamic instrument that uses carbon dioxide gas or fluid to evaluate bladder pressure, volume, and compliance during cystometry. It is an FDA Class 2 device (moderate risk), subject to general controls with no 510(k) required under the applicable submission type. It is regulated under 21 CFR 876.1620 in the Gastroenterology and Urology specialty. No special flags apply.

510(k) Clearances

50+ matches
K Number
Device Name
SIGNAL GEAR URETHRAL CATHETER ELECTRODE
SINGLE CHANNEL UROLOGICAL PRESSURE GAUGE, DUAL CHANNEL UROLOGICAL PRESSURE GAUGE
URODYNAMIC ANALYSIS MODULE
RUSCH URODYNAMIC RECTAL BALLOON 2-WAY CATHETER
SCHUSTER DISPOSABLE BALLOON PROBE
UROLAB SPECTRUM
URO-PRO 2000
SYNECTICS LIBERTY SYSTEM, PC POLYGRAF/POLYGRAM URO
URODYNAMICS TUBING KITS #5161, #5150, #7170
URODYNAMIC CATHETERS
NICKI, MODEL NUMBER USD-NK-UP1
ENDOTEK ULTRA SYSTEM
LABORIE URODYNAMICS PROCESSOR
MERKUR 4000
PHOENIX 5 URODYNAMICS SYSTEM
MODEL 8100 URODYNAMICS MEASURING SYSTEM
IMAGE PRO URODYNAMICS MEASURING SYST, MODIFICATION
PROFILE PLUS URODYNAMICS MEASURING SYST, MODIFIED
URETHRALPRESSURE PROFILE CATHETER
URODYNAMIC CATHETER
DOBBHOFF ANORECT BIOFEED SYST FIVE DIV FECAL CONST
DANTEC UD 5500 MK2
PULLER OPTION FOR ETUDE(TM)
DANTEC MENUET
URODYNAMIC RECTAL BALLOON
ETUDE (MODEL NUMBERS 24A05 & 24A06)
DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020
BROWNE MEDICAL SYSTEMS IMAGEPRO
DIAGNOSTIC ULTRASOUND/URO-GYN UDS 2000 SERIES
URODYNAMIC MEASURING SYSTEM
MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM
BROWNE MEDICAL SYST.INC STAND-ALONE WATER PUMP
BCI-100 FECAL INCONTINENCE SYSTEM
UROLAB JANUS
ETUDE, URODYNAMIC INVESTIGATION SYSTEM
BIOSEARCH ANAL BIOFEEDBACK DEVICE
DIAGNOSTIC ULTRASOUND/URO-GYN UDS 1002
SYNECTICS LIBERTY SYSTEM, PC POLYGRAF & POLYGRAM
DANTEC MENUET
RECTUM-COLON MOTILITY MONITOR
DANTEC 22K60/61/62 CATHETER TIP TRANSDUCER
SURGITEK CO2 DELIVERY SYSTEM
DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODE
13L81 DISPOSABLE SPHINCTER ELECTRODE, 13L33 CABLE
UROSCAN
SANDHILL AMS
MODEL 4-SC FOUR WAY STOPCOCK
MODEL 1101M & 1151M UROLAB MICRO URODYNAMIC RECORD
MODEL 1350 URODYNAMIC WAVEFORM PROCESSOR
MODEL AS-72 ADMINISTRATION SET

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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