You are invited to participate in the Astra Zeneca PACIFIC-9 D9078C00001 study.
This app is specifically intended for study participants in the PACIFIC9 study only.
The Masimo MightySat Rx Pulse (model 9909 or 9907) Oximeter is a Class B digital device, pursuant to part 15 of the FCC Rules and has been been tested and found to comply with the Class B limits for medical devices according to the EN 60601-1-2: 2007, Medical Device Directive 93/42/EEC. The device has Declaration of Comformity (CE) for the following countries: Argentina, Brazil, Canada, Germany, Italy, Japan, Malaysia, Poland, Romania, Singapore, South Korea, Spain, Taiwan, Thailand, Turkey, United Kingdom, and the United States
Disclaimer: Use of this app, sensor, and platform is in the context of a clinical study under the supervision of a physician. Patients should seek advice from their healthcare provider as needed and before making any medical decisions.