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FDA 510(k)

rainbow LS Block

K-Number: K160144 · 2016-07-21

ApplicantGenoss Co., Ltd.
Decision Date2016-07-21
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

rainbow LS Block is a medical device manufactured by Genoss Co., Ltd.. It received FDA 510(k) clearance on 2016-07-21 under approval number K160144. 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 LS Block?

rainbow LS Block is a medical device that received FDA 510(k) clearance on 2016-07-21. It is manufactured by Genoss Co., Ltd.. The 510(k) number is K160144.

When was rainbow LS Block approved by the FDA?

rainbow LS Block received FDA 510(k) clearance on 2016-07-21, under approval number K160144.

What company makes rainbow LS Block?

rainbow LS Block is manufactured by Genoss Co., Ltd..

What is the FDA product code for rainbow LS Block?

The FDA product code for rainbow LS Block is EIH.

Other Devices by Genoss Co., Ltd.

K160079rainbow Shine K153676OSTEON III K170596TN-Brush K200155Bright High Flow K200153Bright Bond Universal K200156Bright Low Flow

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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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