FDA device listing
Alaris/Medley SpO2 Module
FDA device listing 1151532062 · CareFusion 303, INC.
Key facts
| Proprietary names | Alaris/Medley SpO2 Module |
|---|---|
| Owner/operator | CareFusion 303, INC. |
| Owner/operator number | 9068764 |
| Premarket submissions | K010966 |
| Product codes | DQA |
| Device names | DQA - Oximeter |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.2700 |
| Review panels | Cardiovascular |
| Registered establishments | CareFusion 303, INC, CareFusion 303, INC. |
| Establishment registrations | 2016493, 3003879246 |
| FEI numbers | 2016493, 3003879246 |
| Establishment operations | Complaint File Establishment, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database