DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE
K-Number: K023497 · 2002-11-04
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Device Summary
Frequently Asked Questions
What is the DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE?
DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE is a medical device that received FDA 510(k) clearance on 2002-11-04. The listed applicant is Datex-Ohmeda. The 510(k) number is K023497.
When did DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE receive FDA 510(k) clearance?
DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE received FDA 510(k) clearance on 2002-11-04, under 510(k) number K023497.
Who is the listed applicant for DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE?
The FDA 510(k) record lists Datex-Ohmeda as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE?
The FDA product code for DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE is MSX.
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 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: MSX)
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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