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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 a medical device manufactured by Excelsior Resources, LLC. It received FDA 510(k) clearance on 2024-03-20 under approval 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. It is manufactured by Excelsior Resources, LLC. The 510(k) number is K233002.

When was BEED 2,5, BEED 3,8 approved by the FDA?

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

What company makes BEED 2,5, BEED 3,8?

BEED 2,5, BEED 3,8 is manufactured by Excelsior Resources, LLC.

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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