FDA 510(k)

Endobronchial Tube

K号: K152251 · 2016-06-10

申请人Henan Tuoren Medical Device Co., Ltd.

决定日期2016-06-10

产品代码CBI

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器械摘要

Endobronchial Tube is the device name listed in this FDA 510(k) record. The listed applicant is Henan Tuoren Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2016-06-10 under 510(k) number K152251. The device is classified under product code CBI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Endobronchial Tube?

Endobronchial Tube is a medical device that received FDA 510(k) clearance on 2016-06-10. The listed applicant is Henan Tuoren Medical Device Co., Ltd.. The 510(k) number is K152251.

When did Endobronchial Tube receive FDA 510(k) clearance?

Endobronchial Tube received FDA 510(k) clearance on 2016-06-10, under 510(k) number K152251.

Who is the listed applicant for Endobronchial Tube?

The FDA 510(k) record lists Henan Tuoren Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Endobronchial Tube?

The FDA product code for Endobronchial Tube is CBI.

相关器械（代码：CBI）

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器械摘要

常见问题

相关临床试验

相关器械（代码：CBI）

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