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FDA 510(k)

GE DATEX-OHMEDA CENTIVA/5 VENTILATOR

K-Number: K050860 · 2005-06-21

Decision Date2005-06-21
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GE DATEX-OHMEDA CENTIVA/5 VENTILATOR 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 2005-06-21 under 510(k) number K050860. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE DATEX-OHMEDA CENTIVA/5 VENTILATOR?

GE DATEX-OHMEDA CENTIVA/5 VENTILATOR is a medical device that received FDA 510(k) clearance on 2005-06-21. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K050860.

When did GE DATEX-OHMEDA CENTIVA/5 VENTILATOR receive FDA 510(k) clearance?

GE DATEX-OHMEDA CENTIVA/5 VENTILATOR received FDA 510(k) clearance on 2005-06-21, under 510(k) number K050860.

Who is the listed applicant for GE DATEX-OHMEDA CENTIVA/5 VENTILATOR?

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 GE DATEX-OHMEDA CENTIVA/5 VENTILATOR?

The FDA product code for GE DATEX-OHMEDA CENTIVA/5 VENTILATOR is CBK.

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.

View all 59 devices →

Related Devices (Code: CBK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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