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FDA 510(k)

NOBILCAM IMPAK Disc

K号: K251252 · 2025-08-01

决定日期2025-08-01
产品代码MQC
决定实质等同

器械摘要

NOBILCAM IMPAK Disc is the device name listed in this FDA 510(k) record. The listed applicant is Shandong Huge Dental Material Corporation. It received FDA 510(k) clearance on 2025-08-01 under 510(k) number K251252. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

常见问题

What is the NOBILCAM IMPAK Disc?

NOBILCAM IMPAK Disc is a medical device that received FDA 510(k) clearance on 2025-08-01. The listed applicant is Shandong Huge Dental Material Corporation. The 510(k) number is K251252.

When did NOBILCAM IMPAK Disc receive FDA 510(k) clearance?

NOBILCAM IMPAK Disc received FDA 510(k) clearance on 2025-08-01, under 510(k) number K251252.

Who is the listed applicant for NOBILCAM IMPAK Disc?

The FDA 510(k) record lists Shandong Huge Dental Material Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOBILCAM IMPAK Disc?

The FDA product code for NOBILCAM IMPAK Disc is MQC.

相关临床试验

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列明Shandong Huge Dental Material Corporation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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相关器械(代码:MQC)

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

在 FDA 数据库中查看 →

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。

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