FDA 510(k)

HygePLUS 纤维素印模材料

K号: K170812 · 2017-07-26

决定日期2017-07-26

产品代码ELW

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决定实质等同

器械摘要

HygePLUS Alginate Impression Material is the device name listed in this FDA 510(k) record. The listed applicant is Hygedent, Inc.. It received FDA 510(k) clearance on 2017-07-26 under 510(k) number K170812. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the HygePLUS Alginate Impression Material?

HygePLUS Alginate Impression Material is a medical device that received FDA 510(k) clearance on 2017-07-26. The listed applicant is Hygedent, Inc.. The 510(k) number is K170812.

When did HygePLUS Alginate Impression Material receive FDA 510(k) clearance?

HygePLUS Alginate Impression Material received FDA 510(k) clearance on 2017-07-26, under 510(k) number K170812.

Who is the listed applicant for HygePLUS Alginate Impression Material?

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

What is the FDA product code for HygePLUS Alginate Impression Material?

The FDA product code for HygePLUS Alginate Impression Material is ELW.

列明Hygedent, 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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相关器械（代码：ELW）

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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