DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER
K-Number: K002878 · 2000-09-21
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Device Summary
Frequently Asked Questions
What is the DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER?
DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER is a medical device that received FDA 510(k) clearance on 2000-09-21. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K002878.
When did DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER receive FDA 510(k) clearance?
DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER received FDA 510(k) clearance on 2000-09-21, under 510(k) number K002878.
Who is the listed applicant for DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER?
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 DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER?
The FDA product code for DATEX-OHMEDA D-TEC PLUS ANESTHESIA VAPORIZER is CAD.
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: CAD)
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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