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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 the device name listed in this FDA 510(k) record. The listed applicant is Steris. It received FDA 510(k) clearance on 2024-05-31 under 510(k) 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. The listed applicant is Steris. The 510(k) number is K241055.

When did Electro Lube NXT receive FDA 510(k) clearance?

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

Who is the listed applicant for Electro Lube NXT?

The FDA 510(k) record lists Steris as the applicant. This does not by itself establish the device manufacturer.

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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