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: ISD FDA class 2

Exerciser, Measuring

Physical Medicine

View full classification →

A measuring exerciser is a rehabilitation device that combines therapeutic exercise function with measurement capability, allowing clinicians to quantify range of motion, force, or work output during rehabilitation sessions. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is ISD, regulated under 21 CFR 890.5360, within the Physical Medicine medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal Ultra
REAL Immersive System
ActiSpec Activity Monitor
ERGOSELECT/GE
ACTITRAINER
ERGOSELECT 100 K/P, ERGOSELECT 200 K/P
QUINTON MEDTRACK CR PLUS TREADMILL
REHCOR
ULE-2, MULE-2, HAND ACCESSORY KIT
DAVID BACK CLINIC SYSTEM
PHYSIO HAB
SES100
MULE
LORDEX LUMBAR EXTENSION MACHINE
THE BTE WS30
UPPER BODY EXERCISER
STAIR CLIMBER
EXERCISE BICYCLE
HYDRA FITNESS MODEL 311 TOTAL POWER
CARDIO2 CTCKE
STEPMILL EXERCISE SYSTEM
MULTI JOINT WEIGHT SYSTEM MODEL #940-100
CABLE COLUMN WEIGHT SYSTEM MODEL #940-200
TOTAL WORK INTEGRATOR, MODEL #940-110
STAIRMASTER MODEL 6000 ERGOMETER
4000 PT EXERCISE SYSTEM
GAUNTLET STAIR CLIMBER
GRAVITRON UPPER BODY SYSTEM EXERCISER
MONARK ERGOMETERS
FLEXERCYCLE
METABOLIC SYSTEMS
GOLDEN MEAN MACHINE(TM) (CLASS 2)
MEDEX MACHINE
RESUBMITTED EXCALIBUR
UPPERCYCLE STATIONARY EXERCISE MACHINES
DISCIPLINE I
APPLIDYN
PULSESTAR EXERCISE BIKE
R1361 & R1372 MEASURED EXERCISE EQUIPMENT
TORQUE FEEDBACK METER
REMOTE SPEED CONTROL
LODE MODEL CORIVAL ERGOMETER
MFE COUCH ERGOMETER
UNIVERSAL-ERGOTEST
3-D PASSIVE MOBILIZER
STATIONARY EXERCISE BICYCLE
ROTAGYM
CAL-COUNT
COMPUTRIM 900
NUCLEAR STRESS TABLE (NST-1)

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.

Popular Product Codes

Commonly searched