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FDA 510(k)

Ochsner Connected Inhaler Sensor

K号: K223367 · 2023-08-30

决定日期2023-08-30
产品代码CAF
咨询委员会AN 请注意,由于您没有提供完整的医疗设备监管文本,我无法提供完整的翻译。如果您能提供完整的文本,我将很乐意为您翻译。
决定实质等同

器械摘要

Ochsner Connected Inhaler Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Ochsner Clinic Foundation. It received FDA 510(k) clearance on 2023-08-30 under 510(k) number K223367. 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 Ochsner Connected Inhaler Sensor?

Ochsner Connected Inhaler Sensor is a medical device that received FDA 510(k) clearance on 2023-08-30. The listed applicant is Ochsner Clinic Foundation. The 510(k) number is K223367.

When did Ochsner Connected Inhaler Sensor receive FDA 510(k) clearance?

Ochsner Connected Inhaler Sensor received FDA 510(k) clearance on 2023-08-30, under 510(k) number K223367.

Who is the listed applicant for Ochsner Connected Inhaler Sensor?

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

What is the FDA product code for Ochsner Connected Inhaler Sensor?

The FDA product code for Ochsner Connected Inhaler Sensor is CAF.

相关临床试验

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。

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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