Rainbow Shine

Powder, Porcelain

GENOSS Co. Ltd.

The following data is part of a premarket notification filed by Genoss Co. Ltd. with the FDA for Rainbow Shine.

Pre-market Notification Details

• Device ID: K160079
• 510k Number: K160079
• Device Name: Rainbow Shine
• Classification: Powder, Porcelain
• Applicant: GENOSS Co. Ltd. 1F Gyeonggi R&DB Center/226, 2F, GSBC, 105 Gwanggyo-ro Yeongton-gu Suwon-si, KR 443-270
• Contact: Byungsun Kim
• Correspondent: Byungsun Kim; GENOSS Co. Ltd. 1F Gyeonggi R&DB Center/226, 2F, GSBC, 105 Gwanggyo-ro Yeongton-gu Suwon-si, KR 443-270
• Product Code: EIH
• CFR Regulation Number: 872.6660 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2016-01-14
• Decision Date: 2016-11-10
• Summary: summary

NIH GUDID Devices

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