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: DWS FDA class 1

Instruments, Surgical, Cardiovascular

Cardiovascular

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Cardiovascular Surgical Instruments are a category of general-purpose hand tools used by surgeons during cardiovascular procedures, including forceps, scissors, retractors, and other instruments designed specifically for use in the heart and major blood vessels. They are classified as FDA Class 1 devices, representing the lowest level of regulatory concern, and are subject to general controls only. The product code is DWS and these instruments are regulated under 21 CFR 870.4500 within the Cardiovascular medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626
OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)
BURKE CONGENITAL THORACOSCOPY INSTRUMENTS
RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY
G.E. STERILE ANGIOGRAPHIC TRAY
G.E. STERILE CT BIOPSY TRAY
G.E. STERILE DIGITAL ANGIOGRAPHIC TRAY
REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER
HYCULT DIAMOND CORONARY BYPASS KNIFE
INSULATION PAD
MODEL 6888 LEAD TUNNELER
NEWCHILL(TM) CARDIAC INSULATOR
MODIFIED STERILIZATION METHOD OF PTI HEART-LIFT
MODIFIED EXTERNAL PAD
DEKNATEL HIGH PRECISION VASCULAR PUNCH(TM)
PHRENIC NERVE PAD & NERVE PAD W/1/4 PERCARDIAL
PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP
PTI HEART-LIFT(TM) CARDIAC ELEVATOR (STERILE)
METATECH MICROCLIP APPLICATOR
UMI DISPOSABLE BUTTERFLY STYLE PUNCTURE NEEDLE
26MM DIAMETER HANCOCK* TROCAR BLADE AND TIP
PTI HEART-LIFT(TM) CARDIAC SUPPORT SLING (STERILE)
CARDICAD(TM)
BIOSURGE MODEL ILVC-1
CARDIOVASCULAR SURGICAL INSTRUMENTS
MEDSURG CUSTOM CARDIOVASCULAR PROCEDURE TRAY
VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET
SCANLAN TUNNELER, SHEATH & TIP
NAMAN POTTS COURNAND NEEDLE
MANAN SELDINGER NEEDLE
MANAN GWI GUIDE WIRE INTRODUCER
MC-4000 SURGICAL INSTRUMENTS CARDIOVASCULAR
TELEFLEX MEDICAL INTRODUCER NEEDLE
LEMAITRE RETROGRADE VALVULOTOME-MANU-SURGICA INSTR
GORE-TEX TUNNELER
PMA ANGIOGRAPHY TRAY
CATEGORY 1 CIRCULATORY SYSTEM DEVICE
ROTARY VASCULAR KNIFE
LEATHER VALVE CUTTER
SCANLAN SINGLE-USE AORTA PUNCH
KELLY-WICK TANNELER
CARDIAC ELEVATOR
ROTARY VASCULAR KNIFE
LEATHER VALVULOTOME
DEKNATEL DISPOSABLE GOOSEN VASCULAR PNCH
VENOUS CANNULA TRAY
NEOLOOPS
DEKNATEL GOOSEN VASCULAR PUNCH BLADES
AIR ASPIRATOR NEEDLE
HANCOCK AORTIC PUNCH

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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