INSPIRATION VENTILATOR SYSTEM
K-Number: K021112 · 2002-11-22
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Device Summary
Frequently Asked Questions
What is the INSPIRATION VENTILATOR SYSTEM?
INSPIRATION VENTILATOR SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-22. The listed applicant is eVent Medical, Ltd.. The 510(k) number is K021112.
When did INSPIRATION VENTILATOR SYSTEM receive FDA 510(k) clearance?
INSPIRATION VENTILATOR SYSTEM received FDA 510(k) clearance on 2002-11-22, under 510(k) number K021112.
Who is the listed applicant for INSPIRATION VENTILATOR SYSTEM?
The FDA 510(k) record lists eVent Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSPIRATION VENTILATOR SYSTEM?
The FDA product code for INSPIRATION VENTILATOR SYSTEM 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 eVent Medical, Ltd. 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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