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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 the device name listed in this FDA 510(k) record. The listed applicant is Genoss. It received FDA 510(k) clearance on 2016-04-15 under 510(k) 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. The listed applicant is Genoss. The 510(k) number is K151731.

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

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

Who is the listed applicant for Rainbow Paste Stain?

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

What is the FDA product code for Rainbow Paste Stain?

The FDA product code for Rainbow Paste Stain is EIH.

Other records listing Genoss as applicant

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.

View all 16 devices →

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.

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.