KIDNEYvault Portable Renal Perfusion System

FDA 510(k) K234060 · Paragonix Technologies

Substantially Equivalent

510(k) numberK234060

Submission

Device name
KIDNEYvault Portable Renal Perfusion System
Applicant
Paragonix Technologies
Waltham, MA, US
Received
December 22, 2023
Decision date
October 23, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KDN – System, Perfusion, Kidney
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5880
Specialty
Gastroenterology, Urology

Other 510(k)s with product code KDN

510(k)DeviceApplicantDecision
K261644Perfadex PlusKDN · Traditional Xvivo Perfusion AB07/23/2026SE
K260456VI°Port™ Liver Preservation SystemKDN · Traditional Traferox Technologies, Inc.06/01/2026SE
K254305BAROguard Donor Lung Preservation SystemKDN · Special Paragonix Technologies, Inc.01/30/2026SE
K243618EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250)KDN · Traditional Bridge TO Life06/17/2025SE
K243870X°Port Lung Preservation System; X°Port Lung Preservation SolutionKDN · Traditional Traferox Technologies, Inc.05/01/2025SE
K243998DCX Disposable Cassette (DCX)KDN · Traditional Institut Geroges Lopez04/25/2025SE
K243384Belzer UW® Cold Storage Solution (BTLBUW-001)KDN · Traditional Bridge TO Life03/31/2025SE
K243840Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)KDN · Traditional Bridge TO Life03/26/2025SE
K240650LungProtectKDN · Traditional Traferox Technologies, Inc.11/26/2024SE
K230193Servator P Plus SALF SolutionKDN · Traditional S.A.L.F. Spa09/21/2023SE

More from S.A.L.F. Spa

510(k)DeviceDecision
K254305BAROguard Donor Lung Preservation SystemKDN · Special 01/30/2026SE
K223874BAROguardKDN · Traditional 08/15/2023SE
K201048SherpaPak Pediatric Liver Transport SystemKDN · Traditional 07/02/2020SE
K191440Paragonix SherpaPak Pancreas Transport SystemKDN · Traditional 12/20/2019SE
K182735Paragonix SherpaPak Cardiac Transport SystemMSB · Special 10/19/2018SE
K180194SherpaPak Cardiac Transport System and SherpaPak Kidney Transport SystemMSB · Traditional 03/30/2018SE
K143074Sherpa Pak Cardiac Transport SystemMSB · Special 11/25/2014SESK
K143054Sherpa Pak Kidney Transport SystemKDN · Special 11/25/2014SESK
K133694Sherpa Pak TransporterKDN · Traditional 05/23/2014SE
K133432Sherpa Pak Cardiac Transport SystemMSB · Traditional 02/21/2014SE

Questions and answers

When was KIDNEYvault Portable Renal Perfusion System cleared by the FDA?

KIDNEYvault Portable Renal Perfusion System (K234060) received a 510(k) decision of Substantially Equivalent on October 23, 2024, 306 days after the submission was received.

What is the product code of K234060?

The FDA product code is KDN – System, Perfusion, Kidney, a Class II (moderate risk) device regulated under 21 CFR 876.5880.