FDA 510(k)

肺细胞学刷

K号: K182927 · 2020-02-07

决定日期2020-02-07

产品代码BTG

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决定实质等同

器械摘要

Pulmonary Cytology Brush is the device name listed in this FDA 510(k) record. The listed applicant is Hobbs Medical, Inc.. It received FDA 510(k) clearance on 2020-02-07 under 510(k) number K182927. The device is classified under product code BTG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Pulmonary Cytology Brush?

Pulmonary Cytology Brush is a medical device that received FDA 510(k) clearance on 2020-02-07. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K182927.

When did Pulmonary Cytology Brush receive FDA 510(k) clearance?

Pulmonary Cytology Brush received FDA 510(k) clearance on 2020-02-07, under 510(k) number K182927.

Who is the listed applicant for Pulmonary Cytology Brush?

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

What is the FDA product code for Pulmonary Cytology Brush?

The FDA product code for Pulmonary Cytology Brush is BTG.

列明Hobbs Medical, 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。

K241874吸痰导管（2189）

官方来源

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