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: IFP FDA class 1

Formalin, Neutral Buffered

Pathology

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Neutral Buffered Formalin is the most widely used tissue fixative in histopathology, a 10% formaldehyde solution buffered to near-neutral pH to prevent formalin pigment formation, used to preserve biopsy and surgical specimens for routine histological processing and diagnosis. It is regulated as an FDA Class 1 device, the lowest risk level, subject to general controls without requiring premarket notification. The product code is IFP, regulated under 21 CFR 864.4010, in the Pathology medical specialty. This device is exempt from GMP requirements.

510(k) Clearances

15 matches
K Number
Device Name
CONSED FECAL CONCENTRATION SYSTEM
DRY-FORM
(MSI) PATH-SAVER
NBF 10% NEUTRAL BUFFERED FORMALIN
PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN
FORMALIN BUFFERED
CBA FORMALIN
BUF-FIX
FORMALIN SOLUTION 10% NEUTRAL BUFFER
NEUTRAL BUFFERED FORMALIN 10%
MILLONIG'S MODIFIED PHOSPHATE BUFFERED
MILLONIGS MODIFIED PHOSPHATE BUFFERED
10% NEUTRAL BUFFERED FORMALIN CONCENT
NEUTRAL DUFFERED FORMA-SCENT
10% NEUTRAL BUFFERED FORMALDEHYDE

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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