FDA 510(k)

Glidewell® 3DP 牙托树脂

K号: K241493 · 2024-09-12

决定日期2024-09-12

产品代码EBI

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决定实质等同

器械摘要

Glidewell™ 3DP Denture Base Resin is the device name listed in this FDA 510(k) record. The listed applicant is Prismatik Dentalcraft, Inc.. It received FDA 510(k) clearance on 2024-09-12 under 510(k) number K241493. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Glidewell™ 3DP Denture Base Resin?

Glidewell™ 3DP Denture Base Resin is a medical device that received FDA 510(k) clearance on 2024-09-12. The listed applicant is Prismatik Dentalcraft, Inc.. The 510(k) number is K241493.

When did Glidewell™ 3DP Denture Base Resin receive FDA 510(k) clearance?

Glidewell™ 3DP Denture Base Resin received FDA 510(k) clearance on 2024-09-12, under 510(k) number K241493.

Who is the listed applicant for Glidewell™ 3DP Denture Base Resin?

FDA 510(k)记录将Prismatik Dentalcraft, Inc.列为申请人。这本身并不足以确立该设备的制造商。

What is the FDA product code for Glidewell™ 3DP Denture Base Resin?

The FDA product code for Glidewell™ 3DP Denture Base Resin is EBI.

列明Prismatik Dentalcraft, Inc.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。

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官方来源

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