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FDA 510(k)

Rainbow Shine

K-Number: K151842 · 2016-01-14

ApplicantGenoss
Decision Date2016-01-14
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Rainbow Shine is a medical device manufactured by Genoss. It received FDA 510(k) clearance on 2016-01-14 under approval number K151842. 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 Shine?

Rainbow Shine is a medical device that received FDA 510(k) clearance on 2016-01-14. It is manufactured by Genoss. The 510(k) number is K151842.

When was Rainbow Shine approved by the FDA?

Rainbow Shine received FDA 510(k) clearance on 2016-01-14, under approval number K151842.

What company makes Rainbow Shine?

Rainbow Shine is manufactured by Genoss.

What is the FDA product code for Rainbow Shine?

The FDA product code for Rainbow Shine is EIH.

Other Devices by Genoss

K151731Rainbow Paste Stain K151846Rainbow LS Pressing

Related Devices (Code: 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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