FDA 510(k), K111610, TRILOGY SERIES VENTILATOR WITH OXIMETRY
FDA 510(k), K111610, TRILOGY SERIES VENTILATOR WITH OXIMETRY
510(K) Number: K111610
Device Name: TRILOGY SERIES VENTILATOR WITH OXIMETRY
Manufacturer: JOSEPH E OLSAVSKY
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: CBK
Classification Product Code: KXA
Date Received: 06/09/2011
Decision Date: 10/14/2011
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
321 pages (2,871 of 2,550 original pages are fully redacted)
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