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FDA-PMA

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

PMA-Nummer: P210018 · 2022-03-17

Entscheidungsdatum2022-03-17
PMA-NummerP210018
ProduktcodeQSF
GeräteklasseKlasse 3
Medizinische FachrichtungU
BeratungsausschussAN

Produktübersicht

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.

Häufig gestellte Fragen

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.

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