FDA 510(k)

BD Epilor 注射器

K号: K210983 · 2022-05-19

决定日期2022-05-19

产品代码CAZ

咨询委员会AN 请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。

决定实质等同

器械摘要

BD Epilor Syringe 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 2022-05-19 under 510(k) number K210983. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD Epilor Syringe?

BD Epilor Syringe is a medical device that received FDA 510(k) clearance on 2022-05-19. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K210983.

When did BD Epilor Syringe receive FDA 510(k) clearance?

BD Epilor Syringe received FDA 510(k) clearance on 2022-05-19, under 510(k) number K210983.

Who is the listed applicant for BD Epilor Syringe?

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 Epilor Syringe?

The FDA product code for BD Epilor Syringe is CAZ.

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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