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FDA 510(k)

DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02

K-Number: K022507 · 2002-08-23

ApplicantDatex-Ohmeda
Decision Date2002-08-23
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02 is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda. It received FDA 510(k) clearance on 2002-08-23 under 510(k) number K022507. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02?

DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02 is a medical device that received FDA 510(k) clearance on 2002-08-23. The listed applicant is Datex-Ohmeda. The 510(k) number is K022507.

When did DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02 receive FDA 510(k) clearance?

DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02 received FDA 510(k) clearance on 2002-08-23, under 510(k) number K022507.

Who is the listed applicant for DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02?

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 NETWORK AND CENTRAL '02?

The FDA product code for DATEX-OHMEDA S/5 NETWORK AND CENTRAL '02 is MSX.

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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.

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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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