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FDA 510(k)

DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES

K-Number: K992323 · 1999-11-01

ApplicantDatex-Ohmeda, Inc.
Decision Date1999-11-01
Product CodeMLD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda, Inc.. It received FDA 510(k) clearance on 1999-11-01 under 510(k) number K992323. The device is classified under product code MLD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES?

DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1999-11-01. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K992323.

When did DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES receive FDA 510(k) clearance?

DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES received FDA 510(k) clearance on 1999-11-01, under 510(k) number K992323.

Who is the listed applicant for DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES?

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 CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES?

The FDA product code for DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES is MLD.

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Related Devices (Code: MLD)

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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