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FDA 510(k)

Rainbow Paste Stain

K-Number: K151731 · 2016-04-15

ApplicantGenoss
Decision Date2016-04-15
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Rainbow Paste Stain is a medical device manufactured by Genoss. It received FDA 510(k) clearance on 2016-04-15 under approval number K151731. 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?

Rainbow Paste Stain is a medical device that received FDA 510(k) clearance on 2016-04-15. It is manufactured by Genoss. The 510(k) number is K151731.

When was Rainbow Paste Stain approved by the FDA?

Rainbow Paste Stain received FDA 510(k) clearance on 2016-04-15, under approval number K151731.

What company makes Rainbow Paste Stain?

Rainbow Paste Stain is manufactured by Genoss.

What is the FDA product code for Rainbow Paste Stain?

The FDA product code for Rainbow Paste Stain is EIH.

Other Devices by Genoss

K151842Rainbow Shine K151846Rainbow LS Pressing

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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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