FDA 510(k)

BioGuard 空气/水吸阀

K号: K203630 · 2021-01-08

决定日期2021-01-08

产品代码ODC

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决定实质等同

器械摘要

BioGuard Air/Water and Suction Valves is the device name listed in this FDA 510(k) record. The listed applicant is Steris Corporations. It received FDA 510(k) clearance on 2021-01-08 under 510(k) number K203630. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BioGuard Air/Water and Suction Valves?

BioGuard Air/Water and Suction Valves is a medical device that received FDA 510(k) clearance on 2021-01-08. The listed applicant is Steris Corporations. The 510(k) number is K203630.

When did BioGuard Air/Water and Suction Valves receive FDA 510(k) clearance?

BioGuard Air/Water and Suction Valves received FDA 510(k) clearance on 2021-01-08, under 510(k) number K203630.

Who is the listed applicant for BioGuard Air/Water and Suction Valves?

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

What is the FDA product code for BioGuard Air/Water and Suction Valves?

The FDA product code for BioGuard Air/Water and Suction Valves is ODC.

列明Steris Corporations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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