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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: LPZ FDA unclassified

Container, Frozen Donor Tissue Storage

Unknown

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The Frozen Donor Tissue Storage Container is a device used to store frozen biological tissue from human donors, such as bone, skin, or other grafts, under controlled low-temperature conditions to preserve viability until use. This device is currently unclassified (Class U) by the FDA, meaning it has not yet been placed into a final regulatory classification category and its regulatory pathway is pending. The product code is LPZ; no regulation number or specific medical specialty is recorded for this entry. No special flags apply to this device.

510(k) Clearances

6 matches
K Number
Device Name
CRYOBAG, MODEL CB
CRYOBAG
TAMPER HAMPER
ACCESSUS DRY STORAGE PACKAGE STERILE COMP STORAGE
AMPU-PAK
ACCESSUS CRYOPRESERVATION PKG. STERILE TISSUE STOR

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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