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FDA 510(k)

Vasoview Hemopro 3 Power Supply

K-Number: K243918 · 2025-02-26

Decision Date2025-02-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vasoview Hemopro 3 Power Supply is a medical device manufactured by Maquet Cardiovascular, LLC. It received FDA 510(k) clearance on 2025-02-26 under approval number K243918. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vasoview Hemopro 3 Power Supply?

Vasoview Hemopro 3 Power Supply is a medical device that received FDA 510(k) clearance on 2025-02-26. It is manufactured by Maquet Cardiovascular, LLC. The 510(k) number is K243918.

When was Vasoview Hemopro 3 Power Supply approved by the FDA?

Vasoview Hemopro 3 Power Supply received FDA 510(k) clearance on 2025-02-26, under approval number K243918.

What company makes Vasoview Hemopro 3 Power Supply?

Vasoview Hemopro 3 Power Supply is manufactured by Maquet Cardiovascular, LLC.

What is the FDA product code for Vasoview Hemopro 3 Power Supply?

The FDA product code for Vasoview Hemopro 3 Power Supply is GEI.

Other Devices by Maquet Cardiovascular, LLC

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Related Devices (Code: GEI)

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.