FDA 510(k)

Collaboration Live

K号: K212777 · 2021-09-24

决定日期2021-09-24

产品代码LLZ

咨询委员会RA

决定实质等同

器械摘要

Collaboration Live is the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 2021-09-24 under 510(k) number K212777. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Collaboration Live?

Collaboration Live is a medical device that received FDA 510(k) clearance on 2021-09-24. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K212777.

When did Collaboration Live receive FDA 510(k) clearance?

Collaboration Live received FDA 510(k) clearance on 2021-09-24, under 510(k) number K212777.

Who is the listed applicant for Collaboration Live?

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

What is the FDA product code for Collaboration Live?

The FDA product code for Collaboration Live is LLZ.

列明Philips Ultrasound, 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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