ENDURAVENT-5 VENTILATOR
K-Number: K092263 · 2010-01-21
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Device Summary
Frequently Asked Questions
What is the ENDURAVENT-5 VENTILATOR?
ENDURAVENT-5 VENTILATOR is a medical device that received FDA 510(k) clearance on 2010-01-21. The listed applicant is Providence Global Medical, Inc.. The 510(k) number is K092263.
When did ENDURAVENT-5 VENTILATOR receive FDA 510(k) clearance?
ENDURAVENT-5 VENTILATOR received FDA 510(k) clearance on 2010-01-21, under 510(k) number K092263.
Who is the listed applicant for ENDURAVENT-5 VENTILATOR?
The FDA 510(k) record lists Providence Global Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDURAVENT-5 VENTILATOR?
The FDA product code for ENDURAVENT-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 Providence Global Medical, 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.
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
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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