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: GCX FDA class 2

Apparatus, Suction, Operating-Room, Wall Vacuum Powered

General Hospital

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The Apparatus, Suction, Operating-Room, Wall Vacuum Powered (product code GCX) is a wall-vacuum-powered suction system installed in the operating room to aspirate fluids, blood, and debris from the surgical field during procedures, maintaining a clear operative environment. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. The device is regulated under 21 CFR 880.6740 in the General Hospital specialty (HO). No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
STRYKER CASSETTE PUMP
CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEM
SUCTION INSTRUMENTATION
CHASE SUCKER
MEDI-VAC FLEXI-CLEAR SUCTION HANDLE
CURITY THORACENTESIS TRAY
STRYKER SUCTION REGULATOR
RENTON SUCTION DEVICE U.S. PATENT*4,767,404
MEDCARE SUCTION CONNECTING TUBING
CPR YANKAUER
MEDCARE YANKAUER SUCTION DEVICE
STRYKER STRYKEFLOW SUCTION IRRIGATOR (MODIFICATION)
SUCTION TIP CLEANER CUP
NEZHAT-DORSEY SPECIMEN CONTAINER SYSTEM
SSCOR/BOARD ..3 MODEL 23000 PRE-ASSEMBLED SUCTION SYSTEM FOR PATIENT TRANSPORT VEHICLES
INAMED DEVELOPMENT ASPIRATION TIP
OEM MULTI-VAC POWERED SUCTION PUMP
THE MEDIC TM
PLEUR-EVAC(R) ADULT/PEDI DUAL COLL CHEST DRAIN SYS
MEDIVAC
TAHOE SUCTION IRRIGATOR
MODEL SLASE 210 HOLMIUM LASER SYSTEM
SUCTION CONNECTING TUBING
XOMED-TREACE POSITROL FOOTPEDAL SUCTION CONTROL
COOPERSURGICAL MODEL 6080 SMOKE EVACUATOR SYSTEM
LAPAROMED CHOLANGIOGRAM VACUUM DEVICE
THORA-KLEX CHEST DRAINAGE UNIT
CONTAIN(TM)
ACUFLO, VACUUM-POWERED BODY FLUID SUCTION APPARA.
CODMAN SUCTION PATTIE
EQUI-GUARD (ASPIRATOR FILTER)
MANIFOLD
TUBING CONNECTORS
UNIVERSAL POOLE SUCTION TUBE
YANKAUER SUCTION TUBE-RIGID TYPE
YANKAUER SUCTION TUBE-FLEXIBLE TYPE
STOPCOCK
VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM
STERILE SALINE - FOR SUCTION CATHETER LUBRICATION
MECONIUM ASPIRATOR
RECEPTAL (R) SAF-GARD(TM) SUCTION LINER
SUCTION TUBES: HOUSE, BARON
PLEUR-EVAC(R) A-8020--INFANT CHEST DRAINAGE SYSTEM
PLEUR-EVAC(R) A-8000--ADULT/PEDIATRIC CHEST DRAIN
RECEPTAL SAF-GARD(TM) SYSTEM
VAC-RITE
REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES
PLEUR-EVAC(R) A6000 ADULT/PEDIATRIC CHEST DRAINAGE
CONTAIN(TM)
CSPI SPECIMEN TRAP (NON-STERILE)

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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