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: FNJ FDA class 1

Bed, Manual

General Hospital

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The Manual Hospital Bed is a non-powered adjustable bed designed for inpatient use, with position adjustments made by manual cranks to support patient positioning, comfort, and care access. It is classified as FDA Class 1 (lowest risk) and is subject only to general controls. The product code is FNJ, regulated under 21 CFR 880.5120 in the General Hospital specialty. This device is exempt from Good Manufacturing Practice (GMP) requirements.

510(k) Clearances

39 matches
K Number
Device Name
KING KRIB
CRADLE, HOSPITAL BED CLOTHING
BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MAT
SIC 3999 FOLDING ADJUSTABLE HOSPITAL BED
ENVIROTENT (BED)
MSI STANDARD BED MODELS: L1097-64 AND L1085-64
MSI 3003 SERIES BED
MSI 2005 SERIES BED
FOLDING HOSPITAL COT NSN 6530-00-299-8517
PLATFORM MATTRESS W/DISPOSABLE BEDPAN BAG
VSID MEDICAL THREE-FOLDING BED
PENOX HOSPITAL BED
COT, FOLDING, HOSPITAL, ALUMINUM
BED/ADJUST/HOSPITAL/FOLDING FIELD WITHOUT MATTRESS
ROD, IRRIGATOR, SUPPORTING TELESCOPING, TYPE
CART, ORTHOPEDIC BED, STRYKER
ICU/CPU TRANSPORT TRAY
NESBIT EVANS NURSING HOME BED
HOSPITAL BED
COT, FOLDING HOSPITAL ALUMINUM - MANUAL BED
TIPS AND PADS, CANE,CRUTCH AND WALKER
EVEREST & JENNINGS BED MODEL NO. L109564 & L108564
COMBO 36
AM FAB SIDE RAILS MODEL 5000
MERIVAARA HOSPITAL BED
BERNIER ARM SUPPORT
EGERTON TURNING & TILTING NET SUSPEN BED
SIDE RAIL PADS
DEVICE FOR REPOSITIONING A BET PATIENT
GER 540, GER 541 MANUAL BED
SWEEN UNIVERSAL BED RAIL PADS
BED ROCKING DEVICE
THE VERSA-BED
SKIL-CARE BED RAIL PADS
ECHO CARDIOGRAM PAD
TRAPEZE BAR KNOCKED DOWN
TRAPEZE FLOOR BASE
TELESCOPING BEDRAILS
PAD, POLYETHER FOAM, OPEN CELL

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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