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: LHC FDA class 1

Warmer, Irrigation Solution

Physical Medicine

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An irrigation solution warmer is a device used to heat saline or other irrigation fluids to a physiologically appropriate temperature before their use in surgical or physical medicine procedures, reducing patient discomfort and the risk of hypothermia during irrigation. The device is FDA Class 1, the lowest risk category, subject only to general controls and not requiring premarket notification. It carries product code LHC and is regulated under 21 CFR 890.5950 within the Physical Medicine specialty. No special flags apply to this device.

510(k) Clearances

24 matches
K Number
Device Name
Getinge Series Warming Cabinet
ORS-3000LD Slush Drapes, ORS-1000LD Fluid Warming Drapes
IntraTemp Solution Warmer
NON-STERILE ORS-400N SCOPE PILLOW WARMER DRAPE
NON-STERILE ORS WARNING DRAPES/SLUSH+WARMER DISC-DRAPE/SLUSH+WARMER PALTE-DRAPE /FLUID WARMER DRAPE,SKIRTED
INTRATEMP SOLUTION WARMER
SWC/DWC WARMING CABINETS
C CHANGE SOLUTION WARMER
1075LD HUSH-SLUSH
ORS-3000LD
ORS-1000LD
WARMER 2000LD
SSW-STERILE SOLUTION WARMER
UROSURGE UROTHERM FLUID WARMING SYSTEM
WARMETTE
NEZHAT-DORSEY THERMAL RETENTION SYSTEM
CABOT MEDICAL IRRIGATION FLUID WARMER SETS
MODIFICATION OF BAIR HUGGER PATIENT WARMING SYSTEM
ORS-2000 SERIES
C-STAT/1000
THERMAL-PAK MODEL SW 1000
STERILE SOLUTION WARMER
ALPHA-I
AQUACADE

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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