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: KIC FDA class 1

Cushion, Flotation

Physical Medicine

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Flotation Cushion is a pressure-relieving seating device filled with air, gel, or fluid that distributes body weight over a larger surface area to reduce pressure point loading, used in physical medicine and rehabilitation to prevent pressure ulcers in patients with limited mobility or who are wheelchair-dependent. It is classified as FDA Class 1, the lowest risk category, subject to general controls only, meaning it does not require premarket notification or approval. The product code is KIC, regulated under 21 CFR 890.3175, within the Physical Medicine medical specialty.

510(k) Clearances

29 matches
K Number
Device Name
GEL-T CUSHION
PROTEAM CUSHION
CUSTOMCARE SEATING SYSTEM
MULTICURE(R) S GEL PAD
MICOS MICROPULSE(TM) ALTERNATING PRESSURE WHEELCHAIR CUSHION
GEL CUSHION
ZERO-G(TM) GEL/FOAM MATTRESS TOPPER
SAFE-SEAT, LOW-PROFILE WHEELCHAIR CUSHION
C' AIRECUSH SEAT CUSHION
PUSH CUSH
ROHO HEEL PAD
MAXIMUS CUSHION
WHEELCHAIR CUSHIONS
SOF. CARE CUSHION & SOF-CARE CUSHION COVER
PRESSURE RELIEF SEAT CUSHION
ZERO-G
JAY CUSHION
SAFE-SEAT WHEELCHAIR CUSHION
INFLATABLE INVALID RING
ARM CUSHION
RUBBER INFLATABLE RING
WATER FLOATATION PAD
GEL FLOTATION CUSHION
INVALID CUSHION
SILICONE ELBOW, BED AND CHAIR PADS
CONPHAR INVALID RING
SKIL-CARE GEL WEDGE, FLOTATION PAD
CONDUCTIVE CUSHION
FLOTATION UNIT, CHAIR

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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