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: IKK FDA class 2

System, Isokinetic Testing And Evaluation

Physical Medicine

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An Isokinetic Testing and Evaluation System is a device used in Physical Medicine to assess and measure muscular strength, endurance, and power through controlled-speed resistance exercises, commonly used in rehabilitation and sports medicine settings. It is classified as FDA Class 2, representing moderate risk, meaning it requires a 510(k) premarket notification demonstrating substantial equivalence to a predicate device before marketing. The product code is IKK, regulated under 21 CFR 890.1925, within the Physical Medicine medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
AMES THERAPY DEVICE
HUMAC SYSTEM
BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP
CC RIDER, MODEL ME180
CYBEX 770
MOTIVATOR FTR 2000
DEXTER ISOKINETIC
THE BTE DYNAMIC LIFT
CLOSED CHAIN ATTACHMENT, MODEL #820-520
TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR
SINGLE CHAIR INTEGRAL BACK ATTACHMENT
DEXTER HAND EVALUATION AND THERAPY SYSTEM
BIODEX SYSTEM 2 AUTOPROGRAM
BIODEX SYSTEM 2 AUTOPROGRAM
BIODEX,MODEL B-2000
BIODEX SYSTEM 2,MODEL S2-S
MEDX MACHINE
KIN-COM ASYMMETRICAL BACK SYSTEM
CYBEX 6000
TORQUE FRAME QTF1000
PROMATRON 3000
LIDO LINEA
KRONAMAX HUMAN PERFORMANCE LAB
BIODEX LIFT SIMULATOR
LINEAR LIFT DEVICE
CYBEX BACK TESTING AND REHABILITATION SYSTEM
BIODEX BACK SYSTEM ATTACHMENT
MEDX CERVICAL EXTENSION TEST & REHAB MACHINE
TEST ONE
BIO-COORDINATOR SYSTEM
MEDX REHABILITATION MACHINE
LIDO TM ACTIVE BACK
MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO
SIXALYZER
LIDO(TM) WORKSET
LIDO(TM) LIFT
ISOKINETIC SYSTEM, TESTING AND EVALUATION
CYBEX 340
DISCIPLINE II RTD
DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER
LIDO ACTIVE
GRIP STRENGTH DEVICE (GSD)
PORTABLE ISOKINETICS 3001 WRIST/ANKLE UNIT
PORTABLE ISOKINETICS 3004 KNEE UNIT
PORTABLE ISOKINETICS 3005 HIP UNIT
PORTABLE ISOKINETICS 3007 BACK/ABDOMEN UNIT
PORTABLE ISOKINETICS 3002 ISO KANE II
PORTABLE ISOKINETICS 3003 SHOULDER UNIT
TRU-KINETICS (TM)
STATIC STRENGTH TESTER

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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