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FDA 510(k), K093905, TRILOGY 202 VENTILATOR
FDA 510(k), K093905, TRILOGY 202 VENTILATOR
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510(K) Number: K093905
Device Name: TRILOGY 202 VENTILATOR
Manufacturer: RESPIRONICS, INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 12/22/2009
Decision Date: 05/12/2010
Regulation Medical Specialty: Anesthesiology
Device Name: TRILOGY 202 VENTILATOR
Manufacturer: RESPIRONICS, INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 12/22/2009
Decision Date: 05/12/2010
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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