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FDA 510(k)

Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert 三角尖端, Contour P-Insert WC 尖端, Contour P-Insert 四尖尖端

K号: K192033 · 2020-06-09

决定日期2020-06-09
产品代码DZI
咨询委员会DE 请注意,您没有提供具体的医疗设备监管文本内容,因此我无法进行翻译。请提供需要翻译的具体文本,我将根据您的要求进行翻译。
决定实质等同

器械摘要

Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip is the device name listed in this FDA 510(k) record. The listed applicant is Bennett Jacoby, Dds, Ms, Inc.. It received FDA 510(k) clearance on 2020-06-09 under 510(k) number K192033. The device is classified under product code DZI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip?

Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip is a medical device that received FDA 510(k) clearance on 2020-06-09. The listed applicant is Bennett Jacoby, Dds, Ms, Inc.. The 510(k) number is K192033.

When did Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip receive FDA 510(k) clearance?

Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip received FDA 510(k) clearance on 2020-06-09, under 510(k) number K192033.

Who is the listed applicant for Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip?

The FDA 510(k) record lists Bennett Jacoby, Dds, Ms, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip?

The FDA product code for Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip is DZI.

相关临床试验

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。

相关器械(代码:DZI)

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。

官方来源

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