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FDA PMA

麻醉气体机软件选项,以实现并维持目标呼气末氧和麻醉剂。

PMA编号:P210018 · 2022-03-17

决定日期2022-03-17
PMA 编号P210018
产品代码QSF
设备分类第3类
医疗专科U
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。

器械摘要

Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda, Inc., A General Electric Company. It received FDA 510(k) clearance on 2022-03-17. The device is classified under product code QSF. It was reviewed by the AN advisory panel.

常见问题

What is the Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents?

Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents is a medical device that received FDA 510(k) clearance on 2022-03-17. The listed applicant is Datex-Ohmeda, Inc., A General Electric Company.

When did Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents receive FDA 510(k) clearance?

The clearance date for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents can be found in the official FDA records.

Who is the listed applicant for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents?

The FDA 510(k) record lists Datex-Ohmeda, Inc., A General Electric Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents?

The FDA product code for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents is QSF.

相关临床试验

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