Glass Ceramic
K-Number: K223194 · 2023-02-10
ApplicantShenzhen Xiangtong Co., Ltd.
Decision Date2023-02-10
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Glass Ceramic is a medical device manufactured by Shenzhen Xiangtong Co., Ltd.. It received FDA 510(k) clearance on 2023-02-10 under approval number K223194. 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 Ceramic?
Glass Ceramic is a medical device that received FDA 510(k) clearance on 2023-02-10. It is manufactured by Shenzhen Xiangtong Co., Ltd.. The 510(k) number is K223194.
When was Glass Ceramic approved by the FDA?
Glass Ceramic received FDA 510(k) clearance on 2023-02-10, under approval number K223194.
What company makes Glass Ceramic?
Glass Ceramic is manufactured by Shenzhen Xiangtong Co., Ltd..
What is the FDA product code for Glass Ceramic?
The FDA product code for Glass Ceramic is EIH.
Related Clinical Trials
Other Devices by Shenzhen Xiangtong 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.