FDA device listing
Aspire Subglottic Suction Endotracheal Tube
FDA device listing 1464511069 · NeVap Inc
Key facts
| Proprietary names | Aspire Subglottic Suction Endotracheal Tube |
|---|---|
| Owner/operator | NeVap Inc |
| Owner/operator number | 10057984 |
| Premarket submissions | K172208 |
| Product codes | BSR, BTR |
| Device names | BSR - Stylet, Tracheal Tube, BTR - Tube, Tracheal (W/Wo Connector) |
| Device class | Class I, Class II |
| Classification regulations (21 CFR) | 868.5730, 868.5790 |
| Review panels | Anesthesiology |
| Registered establishments | NeVap Inc Inventory Management |
| Establishment registrations | 3014544429 |
| FEI numbers | 3014544429 |
| Establishment operations | Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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