FDA 510(k)

bioli lOL输送系统

K号: K200057 · 2020-06-04

决定日期2020-06-04

产品代码MSS

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决定实质等同

器械摘要

bioli lOL Delivery System is the device name listed in this FDA 510(k) record. The listed applicant is Ast Products, Inc.. It received FDA 510(k) clearance on 2020-06-04 under 510(k) number K200057. The device is classified under product code MSS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the bioli lOL Delivery System?

bioli lOL Delivery System is a medical device that received FDA 510(k) clearance on 2020-06-04. The listed applicant is Ast Products, Inc.. The 510(k) number is K200057.

When did bioli lOL Delivery System receive FDA 510(k) clearance?

bioli lOL Delivery System received FDA 510(k) clearance on 2020-06-04, under 510(k) number K200057.

Who is the listed applicant for bioli lOL Delivery System?

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

What is the FDA product code for bioli lOL Delivery System?

The FDA product code for bioli lOL Delivery System is MSS.

列明Ast Products, 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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官方来源

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