Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Coloring Liquid

K-Number: K192723 · 2020-08-18

Decision Date2020-08-18
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Coloring Liquid is the device name listed in this FDA 510(k) record. The listed applicant is Aidite (Qinhuangdao) Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-08-18 under 510(k) number K192723. 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 Coloring Liquid?

Coloring Liquid is a medical device that received FDA 510(k) clearance on 2020-08-18. The listed applicant is Aidite (Qinhuangdao) Technology Co., Ltd.. The 510(k) number is K192723.

When did Coloring Liquid receive FDA 510(k) clearance?

Coloring Liquid received FDA 510(k) clearance on 2020-08-18, under 510(k) number K192723.

Who is the listed applicant for Coloring Liquid?

The FDA 510(k) record lists Aidite (Qinhuangdao) Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Coloring Liquid?

The FDA product code for Coloring Liquid is EIH.

Other records listing Aidite (Qinhuangdao) Technology Co., Ltd. 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.