FDA 510(k)

Kingcera Dental Zirconia Blank

K号: K241602 · 2024-08-30

申请人Hunan Qinghao Puzhong Technology Co., Ltd.

决定日期2024-08-30

产品代码EIH

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决定实质等同

器械摘要

Kingcera Dental Zirconia Blank is the device name listed in this FDA 510(k) record. The listed applicant is Hunan Qinghao Puzhong Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-08-30 under 510(k) number K241602. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Kingcera Dental Zirconia Blank?

Kingcera Dental Zirconia Blank is a medical device that received FDA 510(k) clearance on 2024-08-30. The listed applicant is Hunan Qinghao Puzhong Technology Co., Ltd.. The 510(k) number is K241602.

When did Kingcera Dental Zirconia Blank receive FDA 510(k) clearance?

Kingcera Dental Zirconia Blank received FDA 510(k) clearance on 2024-08-30, under 510(k) number K241602.

Who is the listed applicant for Kingcera Dental Zirconia Blank?

FDA 510(k)记录将湖南清毫普众科技有限公司列为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Kingcera Dental Zirconia Blank?

The FDA product code for Kingcera Dental Zirconia Blank is EIH.

列明Hunan Qinghao Puzhong Technology Co., Ltd.为申报人的其他记录

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