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: DRO FDA class 2

Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

Cardiovascular

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The External Transcutaneous (Non-Invasive) Cardiac Pacemaker is a cardiovascular device used to deliver electrical stimulation to the heart through electrodes placed on the surface of the skin, providing temporary pacing support without the need for vascular access. It is classified as an FDA Class 2 device, indicating moderate risk, and requires 510(k) premarket notification before marketing. The product code is DRO and it is regulated under 21 CFR 870.5550 within the Cardiovascular medical specialty. This device is designated as life-sustaining or life-supporting.

510(k) Clearances

50+ matches
K Number
Device Name
K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85
LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODES
ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413
PADTAK PACE/DEFIB/CARDIOVERT MONITORING ELECTRODE(S)
PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERT
PORTABLE INTENSIVE CARE UNIT
CARDIOSERV P
RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM
ESORT II + 400 SERIES MONITOR
ZOLL PD2000 PACEMAKER/ADVISORY DEFIBRILLATOR, MODEL PD2000, ZOLL D2000 ADVISORY DEFIBRILLATOR, MODEL D2000
LIFEPAK 11
HEWLETT PACKARD M2475B CODEMASTER 100 DEFIBRILLATOR/MONITOR
K-DEFIB/PACE CARBON ELECTRODE
MODELS M1722A, M1723A, M1724A DEFIBRILLATORS
GEL-TAC
K-DEFIB/PACE ELECTRODE
QUIK-PACE(R) OR EX-PACE(TM) PEDIATRIC PACING ELEC
ZOLL PD-1400 PACER/DEFIBRILLATOR
MODEL 205 SHOCK-TRODE
DISPOS ACCESS EXTERNAL CARDIAC PACEMAKER
NKA MODEL SEC-3102 CARDIAC STIMULATOR
DEFIB/PACING PADS
R2 PACE PAD, MODEL 480
R2 PACE ADAPTOR CABLE, MODEL 196
ZMI PART NO. NTP-2100, PEDIATRIC ELECTRODES
MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE
MRL PACETTE, 450SLL
TRIAD-EP II, PUSHBUTTON, CABLE INPUT
TRIAD-EP II, PLATE INPUT
TRIAD-EP, PUSHBUTTON, CABLE INPUT TYPE
TRAID-EP, PLATE INPUT, W/PULSE BLANKING CIRCUITRY
TRIAD-EP, PUSHBUTTON, CABLE INPUT TYPE, W/PULSE
QUIK-PACE II ELECTRODES
MODEL #918 MULTI-PADS
MODEL #716 ADULT STIM. PADS LOW IMPEDANCE GEL TYPE
EXTERNAL PACEMAKER 2000 (EP2000)
TRIAD-EP
DISPOSABLE GEL DEFIBRILLATION/EXTERNAL PACING ELEC
QUIK-PACE NONINVASIVE PACEMAKER
300M ECG MONITRO/TRANSCUTANEOUS PACEMAKER
ZOLL NTP-1200 PACER/DEFIBRILLATOR
PACESTART
MODIFIED VERSA STIM ELECTRODE LINE
LECTEC NON-INVASIVE PACING ELECTRODE
STAT-PAD (TM)
MODIFIED PACE*AID MODEL 53
MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR
PACE 10 NON-INVASIVE EXTERNAL PACEMAKER
DISPOS GEL EXTERNAL PACING ELECTRODE/LOW IMPEDANCE
DISPOS GEL EXTERNAL PACING ELECTRODE/HI IMPEDANCE

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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