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FDA 510(k)

rainbow Paste Stain SE

K-Number: K233885 · 2024-06-21

ApplicantGenoss Co., Ltd.
Decision Date2024-06-21
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

rainbow Paste Stain SE is a medical device manufactured by Genoss Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under approval number K233885. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the rainbow Paste Stain SE?

rainbow Paste Stain SE is a medical device that received FDA 510(k) clearance on 2024-06-21. It is manufactured by Genoss Co., Ltd.. The 510(k) number is K233885.

When was rainbow Paste Stain SE approved by the FDA?

rainbow Paste Stain SE received FDA 510(k) clearance on 2024-06-21, under approval number K233885.

What company makes rainbow Paste Stain SE?

rainbow Paste Stain SE is manufactured by Genoss Co., Ltd..

What is the FDA product code for rainbow Paste Stain SE?

The FDA product code for rainbow Paste Stain SE is EIH.

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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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