FDA device listing
WVSM RWC + miniCap
FDA device listing 1653255346 · Athena GTX
Key facts
| Proprietary names | WVSM RWC + miniCap |
|---|---|
| Owner/operator | Athena GTX |
| Owner/operator number | 10034326 |
| Premarket submissions | K191989 |
| Product codes | CCK, DQA, DRG, DXN, MWI |
| Device names | CCK - Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, DQA - Oximeter, DRG - Transmitters And Receivers, Physiological Signal, Radiofrequency, DXN - System, Measurement, Blood-Pressure, Non-Invasive, MWI - Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.1400, 870.1130, 870.2300, 870.2700, 870.2910 |
| Review panels | Anesthesiology, Cardiovascular |
| Registered establishments | ATHENA GTX |
| Establishment registrations | 3007413079 |
| FEI numbers | 3007413079 |
| Establishment operations | Complaint File Establishment, Manufacturer, Remanufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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