AESPIRE 7900, AESPIRE VIEW
K-Number: K092864 · 2010-01-12
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Device Summary
Frequently Asked Questions
What is the AESPIRE 7900, AESPIRE VIEW?
AESPIRE 7900, AESPIRE VIEW is a medical device that received FDA 510(k) clearance on 2010-01-12. The listed applicant is Datex-Ohmeda Inc., A Division of Instrumentarium C. The 510(k) number is K092864.
When did AESPIRE 7900, AESPIRE VIEW receive FDA 510(k) clearance?
AESPIRE 7900, AESPIRE VIEW received FDA 510(k) clearance on 2010-01-12, under 510(k) number K092864.
Who is the listed applicant for AESPIRE 7900, AESPIRE VIEW?
The FDA 510(k) record lists Datex-Ohmeda Inc., A Division of Instrumentarium C as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AESPIRE 7900, AESPIRE VIEW?
The FDA product code for AESPIRE 7900, AESPIRE VIEW 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., A Division of Instrumentarium C 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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