FDA device listing
Salter Labs® Percent-O2-Lock® Venturi System
FDA device listing 1792208592 · SunMed "also trading as AirLife"
Key facts
| Proprietary names | Salter Labs® Percent-O2-Lock® Venturi System |
|---|---|
| Owner/operator | SunMed "also trading as AirLife" |
| Owner/operator number | 9038422 |
| Premarket submissions | K772127 |
| Product codes | BYF |
| Device names | BYF - Mask, Oxygen, Low Concentration, Venturi |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5600 |
| Review panels | Anesthesiology |
| Registered establishments | Salter Labs, Salter Labs de Mexico de S.A. de C.V. |
| Establishment registrations | 3004748541, 3010272829 |
| FEI numbers | 3004748541, 3010272829 |
| Establishment operations | Manufacturer, 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