Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents
Numéro PMA : P210018 · 2022-03-17
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Questions fréquentes
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.
Essais cliniques associés
Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.
Source officielle
Voir dans la base de données FDA →Données issues de l'API ouverte de la FDA. Pour les informations les plus récentes et faisant autorité, veuillez toujours vous référer au registre officiel.
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