FDA 510(k)

Gem FlowCoupler System

K号: K191252 · 2019-07-09

申请人Baxter/ Synovis Micro Companies Alliance, Inc.

决定日期2019-07-09

产品代码MVR

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决定实质等同

器械摘要

Gem FlowCoupler System is the device name listed in this FDA 510(k) record. The listed applicant is Baxter/ Synovis Micro Companies Alliance, Inc.. It received FDA 510(k) clearance on 2019-07-09 under 510(k) number K191252. The device is classified under product code MVR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Gem FlowCoupler System?

Gem FlowCoupler System is a medical device that received FDA 510(k) clearance on 2019-07-09. The listed applicant is Baxter/ Synovis Micro Companies Alliance, Inc.. The 510(k) number is K191252.

When did Gem FlowCoupler System receive FDA 510(k) clearance?

Gem FlowCoupler System received FDA 510(k) clearance on 2019-07-09, under 510(k) number K191252.

Who is the listed applicant for Gem FlowCoupler System?

The FDA 510(k) record lists Baxter/ Synovis Micro Companies Alliance, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Gem FlowCoupler System?

The FDA product code for Gem FlowCoupler System is MVR.

列明Baxter/ Synovis Micro Companies Alliance, 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。

K190499Gem FlowCoupler System

官方来源

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