FDA 510(k)

The Slide

K号: K203712 · 2021-07-20

决定日期2021-07-20

产品代码LQZ

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决定实质等同

器械摘要

The Slide is the device name listed in this FDA 510(k) record. The listed applicant is Biotex, Inc.. It received FDA 510(k) clearance on 2021-07-20 under 510(k) number K203712. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the The Slide?

The Slide is a medical device that received FDA 510(k) clearance on 2021-07-20. The listed applicant is Biotex, Inc.. The 510(k) number is K203712.

When did The Slide receive FDA 510(k) clearance?

The Slide received FDA 510(k) clearance on 2021-07-20, under 510(k) number K203712.

Who is the listed applicant for The Slide?

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

What is the FDA product code for The Slide?

The FDA product code for The Slide is LQZ.

列明Biotex, 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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