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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 the device name listed in this FDA 510(k) record. The listed applicant is Genoss Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) 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. The listed applicant is Genoss Co., Ltd.. The 510(k) number is K233885.

When did rainbow Paste Stain SE receive FDA 510(k) clearance?

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

Who is the listed applicant for rainbow Paste Stain SE?

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

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

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

Other records listing Genoss Co., Ltd. as applicant

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Related Devices (Code: EIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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