FDA 510(k)

Reprocessed Compression Garments

K号: K161105 · 2016-08-18

决定日期2016-08-18

产品代码JOW

咨询委员会CV

决定Substantially Equivalent

器械摘要

Reprocessed Compression Garments is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2016-08-18 under 510(k) number K161105. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Reprocessed Compression Garments?

Reprocessed Compression Garments is a medical device that received FDA 510(k) clearance on 2016-08-18. The listed applicant is Covidien. The 510(k) number is K161105.

When did Reprocessed Compression Garments receive FDA 510(k) clearance?

Reprocessed Compression Garments received FDA 510(k) clearance on 2016-08-18, under 510(k) number K161105.

Who is the listed applicant for Reprocessed Compression Garments?

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

What is the FDA product code for Reprocessed Compression Garments?

The FDA product code for Reprocessed Compression Garments is JOW.

列明Covidien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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