GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM
K-Number: K050626 · 2005-03-25
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Device Summary
Frequently Asked Questions
What is the GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM?
GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM is a medical device that received FDA 510(k) clearance on 2005-03-25. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K050626.
When did GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM receive FDA 510(k) clearance?
GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM received FDA 510(k) clearance on 2005-03-25, under 510(k) number K050626.
Who is the listed applicant for GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM?
The FDA 510(k) record lists Datex-Ohmeda, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM?
The FDA product code for GE DATEX-OHMEDA AESPIRE 7900 ANESTHESIA SYSTEM is BSZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Datex-Ohmeda, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BSZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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