TRILOGY 202 VENTILATOR
K-Number: K093905 · 2010-05-12
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Device Summary
Frequently Asked Questions
What is the TRILOGY 202 VENTILATOR?
TRILOGY 202 VENTILATOR is a medical device that received FDA 510(k) clearance on 2010-05-12. The listed applicant is Respironics, Inc.. The 510(k) number is K093905.
When did TRILOGY 202 VENTILATOR receive FDA 510(k) clearance?
TRILOGY 202 VENTILATOR received FDA 510(k) clearance on 2010-05-12, under 510(k) number K093905.
Who is the listed applicant for TRILOGY 202 VENTILATOR?
The FDA 510(k) record lists Respironics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRILOGY 202 VENTILATOR?
The FDA product code for TRILOGY 202 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 Respironics, 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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