Glass Ceramics
K-Number: K222513 · 2023-02-10
Decision Date2023-02-10
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Glass Ceramics is a medical device manufactured by Yilink (Tianjin) Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2023-02-10 under approval number K222513. 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 Glass Ceramics?
Glass Ceramics is a medical device that received FDA 510(k) clearance on 2023-02-10. It is manufactured by Yilink (Tianjin) Biotechnology Co., Ltd.. The 510(k) number is K222513.
When was Glass Ceramics approved by the FDA?
Glass Ceramics received FDA 510(k) clearance on 2023-02-10, under approval number K222513.
What company makes Glass Ceramics?
Glass Ceramics is manufactured by Yilink (Tianjin) Biotechnology Co., Ltd..
What is the FDA product code for Glass Ceramics?
The FDA product code for Glass Ceramics is EIH.
Other Devices by Yilink (Tianjin) Biotechnology Co., Ltd.
Related Devices (Code: EIH)
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.