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FDA 510(k)

Advanced Skin Renewing Device

K-Number: K182498 · 2018-11-30

ApplicantJiangsu Unimed Laser Technology Co., Ltd.
Decision Date2018-11-30
Product CodeONG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Advanced Skin Renewing Device is a medical device manufactured by Jiangsu Unimed Laser Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-11-30 under approval number K182498. The device is classified under product code ONG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Advanced Skin Renewing Device?

Advanced Skin Renewing Device is a medical device that received FDA 510(k) clearance on 2018-11-30. It is manufactured by Jiangsu Unimed Laser Technology Co., Ltd.. The 510(k) number is K182498.

When was Advanced Skin Renewing Device approved by the FDA?

Advanced Skin Renewing Device received FDA 510(k) clearance on 2018-11-30, under approval number K182498.

What company makes Advanced Skin Renewing Device?

Advanced Skin Renewing Device is manufactured by Jiangsu Unimed Laser Technology Co., Ltd..

What is the FDA product code for Advanced Skin Renewing Device?

The FDA product code for Advanced Skin Renewing Device is ONG.

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Related PubMed Literature

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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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