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FDA 510(k)

BEED 2,5, BEED 3,8

K-Number: K233002 · 2024-03-20

ApplicantExcelsior Resources, LLC
Decision Date2024-03-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BEED 2,5, BEED 3,8 is the device name listed in this FDA 510(k) record. The listed applicant is Excelsior Resources, LLC. It received FDA 510(k) clearance on 2024-03-20 under 510(k) number K233002. 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 BEED 2,5, BEED 3,8?

BEED 2,5, BEED 3,8 is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Excelsior Resources, LLC. The 510(k) number is K233002.

When did BEED 2,5, BEED 3,8 receive FDA 510(k) clearance?

BEED 2,5, BEED 3,8 received FDA 510(k) clearance on 2024-03-20, under 510(k) number K233002.

Who is the listed applicant for BEED 2,5, BEED 3,8?

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

What is the FDA product code for BEED 2,5, BEED 3,8?

The FDA product code for BEED 2,5, BEED 3,8 is GEI.

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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.

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