FDA 510(k)

BD BACTEC™ Plus 好氧/F 培养管

K号: K222591 · 2023-03-24

决定日期2023-03-24

产品代码MDB

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决定实质等同

器械摘要

BD BACTEC™ Plus Aerobic/F Culture Vials is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2023-03-24 under 510(k) number K222591. The device is classified under product code MDB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD BACTEC™ Plus Aerobic/F Culture Vials?

BD BACTEC™ Plus Aerobic/F Culture Vials is a medical device that received FDA 510(k) clearance on 2023-03-24. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K222591.

When did BD BACTEC™ Plus Aerobic/F Culture Vials receive FDA 510(k) clearance?

BD BACTEC™ Plus Aerobic/F Culture Vials received FDA 510(k) clearance on 2023-03-24, under 510(k) number K222591.

Who is the listed applicant for BD BACTEC™ Plus Aerobic/F Culture Vials?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD BACTEC™ Plus Aerobic/F Culture Vials?

The FDA product code for BD BACTEC™ Plus Aerobic/F Culture Vials is MDB.

列明Becton, Dickinson and Company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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