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: GAA FDA class 1

Needle, Aspiration And Injection, Disposable

General, Plastic Surgery

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The Needle, Aspiration And Injection, Disposable (product code GAA) is a single-use needle designed for both aspirating fluid from or injecting fluid into tissue or body cavities during general and plastic surgery procedures. It is classified as FDA Class 1, the lowest risk level, subject only to general controls and not requiring premarket notification. The device is regulated under 21 CFR 878.4800 in the General, Plastic Surgery specialty (SU). No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
CapnoSpot™ Pneumothorax Decompression Indicator
ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT
IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGE
PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES
INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX
MANAN ACCURA NEEDLE
BONOPTY COAXIAL BONE BIOPSY SYSTEM WITH ECCENTRIC DRILL(10-1072,3,4)
MD TECH BIOPSY SET FOR BONE AND BONE MARROW
MONOJECT BONE MARROW BIOPSY TRAYS
MANAN GENERAL PURPOSE INTRODUCER NEEDLE
MANAN BONE MARROW HARVEST NEEDLES
BONE MARROW BIOPSY PROCEDURE TRAY
IRRIGATION/ASPIRATION TUBING SET
GILLAM-TUKEL BONE MARROW BIOPSY NEEDLE
SYMBIOSIS BONE MARROW BIOPSY NEEDLE
TURKEL THORACENTESIS SYSTEM
KOPAN'S TARGET
BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120
ASPIRATION/INJECTION NEEDLE
BONE MARROW BIOPSY TRAY
SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES
REDDICK IRRIGATION/ASPIRATION SYSTEM
SURE-STOP TRANSBRONCHIAL ASPIRATION NEEDLE
WILSON-COOK LUNG BIOPSY NEEDLE
KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG)
JACKSON FINE NEEDLE ASPIRATION SYSTEM
MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.
E-Z-EM VACUUM ASPIRATION SYRINGE
16 GA X 10 BULLET POINT NEEDLE
16 GA X 6 BULLET POINT NEEDLE
20GA X 7-1/2 THREADING BULLET POINT NEEDLE
14 INCH BULLET POINT NEEDLE
THORACENTISIS KIT
MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED
CODE #D2020-FINE NEEDLE ASPIRATION BIOPSY SYSTEM
NOVO VIVO MODEL #17140 AND #17135
PRIA-KIT (TM) PRIAPISM KIT S.S.
ANCHOR BIOPSY NEEDLE
MEDSURG CHIBA PTC NEEDLE
NOTCH-NEEDLE, WESCOTT STYLE
NAMIC CHIBA ASPIRATION BIOPSY NEEDLE
RANFAC CUT BIOPSY NEEDLE
MANAN BREST TUMOR LOCALIZATION NEEDLE
BONE MARROW TRAY
TBI NEEDLE
ANGIOMED FINE NEEDLES AND NEEDLE SET
HYPODERMIC NEEDLE AND STYLET
NEEDLE W/STYLET FOR IMPLANTATION
EROSA DISPOSABLE HYPODERMIC NEEDLE
LEE BONE MARROW BIOPSY/ASPIRATION TRAY

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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