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FDA 510(k)

Electro Lube NXT

K-Number: K241055 · 2024-05-31

ApplicantSteris
Decision Date2024-05-31
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Electro Lube NXT is a medical device manufactured by Steris. It received FDA 510(k) clearance on 2024-05-31 under approval number K241055. 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 Electro Lube NXT?

Electro Lube NXT is a medical device that received FDA 510(k) clearance on 2024-05-31. It is manufactured by Steris. The 510(k) number is K241055.

When was Electro Lube NXT approved by the FDA?

Electro Lube NXT received FDA 510(k) clearance on 2024-05-31, under approval number K241055.

What company makes Electro Lube NXT?

Electro Lube NXT is manufactured by Steris.

What is the FDA product code for Electro Lube NXT?

The FDA product code for Electro Lube NXT is GEI.

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Official Source

View on FDA Database →

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

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