FDA 510(k)

DBSWIN, VISTAEASY

K号: K203287 · 2020-11-18

决定日期2020-11-18

产品代码LLZ

咨询委员会RA

决定实质等同

器械摘要

DBSWIN, VISTAEASY is the device name listed in this FDA 510(k) record. The listed applicant is Dürr Dental SE. It received FDA 510(k) clearance on 2020-11-18 under 510(k) number K203287. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the DBSWIN, VISTAEASY?

DBSWIN, VISTAEASY is a medical device that received FDA 510(k) clearance on 2020-11-18. The listed applicant is Dürr Dental SE. The 510(k) number is K203287.

When did DBSWIN, VISTAEASY receive FDA 510(k) clearance?

DBSWIN, VISTAEASY received FDA 510(k) clearance on 2020-11-18, under 510(k) number K203287.

Who is the listed applicant for DBSWIN, VISTAEASY?

FDA 510(k)记录显示Dürr Dental SE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 DBSWIN, VISTAEASY?

The FDA product code for DBSWIN, VISTAEASY is LLZ.

列明Dürr Dental SE为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K262073卫生防护咬合盖（2207-010-50）K202633ScanX边缘

官方来源

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数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。