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FDA 510(k)

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)

K-Number: K243840 · 2025-03-26

Decision Date2025-03-26
Product CodeKDN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) is a medical device manufactured by Bridge TO Life. It received FDA 510(k) clearance on 2025-03-26 under approval number K243840. The device is classified under product code KDN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)?

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) is a medical device that received FDA 510(k) clearance on 2025-03-26. It is manufactured by Bridge TO Life. The 510(k) number is K243840.

When was Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) approved by the FDA?

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) received FDA 510(k) clearance on 2025-03-26, under approval number K243840.

What company makes Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)?

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) is manufactured by Bridge TO Life.

What is the FDA product code for Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)?

The FDA product code for Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) is KDN.

Related Clinical Trials

Other Devices by Bridge TO Life

Related Devices (Code: KDN)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.