Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX

K-Number: K012531 · 2001-11-02

ApplicantDatex-Ohmeda
Decision Date2001-11-02
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda. It received FDA 510(k) clearance on 2001-11-02 under 510(k) number K012531. 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 DEVICE INTERFACING SOLUTION, N-DISXXXX?

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX is a medical device that received FDA 510(k) clearance on 2001-11-02. The listed applicant is Datex-Ohmeda. The 510(k) number is K012531.

When did DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX receive FDA 510(k) clearance?

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX received FDA 510(k) clearance on 2001-11-02, under 510(k) number K012531.

Who is the listed applicant for DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX?

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 DEVICE INTERFACING SOLUTION, N-DISXXXX?

The FDA product code for DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX 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.

View all 41 devices →

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.

↑