FDA 510(k)

Propeller 传感器用于 Symbicort

K号: K192724 · 2020-03-26

决定日期2020-03-26

产品代码CAF

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决定实质等同

器械摘要

Propeller Sensor for Symbicort is the device name listed in this FDA 510(k) record. The listed applicant is Reciprocal Labs Corporation. It received FDA 510(k) clearance on 2020-03-26 under 510(k) number K192724. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Propeller Sensor for Symbicort?

Propeller Sensor for Symbicort is a medical device that received FDA 510(k) clearance on 2020-03-26. The listed applicant is Reciprocal Labs Corporation. The 510(k) number is K192724.

When did Propeller Sensor for Symbicort receive FDA 510(k) clearance?

Propeller Sensor for Symbicort received FDA 510(k) clearance on 2020-03-26, under 510(k) number K192724.

Who is the listed applicant for Propeller Sensor for Symbicort?

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

What is the FDA product code for Propeller Sensor for Symbicort?

The FDA product code for Propeller Sensor for Symbicort is CAF.

列明Reciprocal Labs Corporation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。

K180770Propeller 传感器用于 Neohaler K161454Propeller 传感器型号 2015-E

相关器械（代码：CAF）

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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