FDA device listing
AGACHAMBER SPACER EXTRA
FDA device listing 1436531612 · AGAPLASTIC IND. COM. LTDA.
Key facts
| Proprietary names | AGACHAMBER SPACER EXTRA |
|---|---|
| Owner/operator | AGAPLASTIC IND. COM. LTDA. |
| Owner/operator number | 9040469 |
| Premarket submissions | K101348 |
| Product codes | NVP |
| Device names | NVP - Holding Chambers, Direct Patient Interface |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.5630 |
| Review panels | Anesthesiology |
| Registered establishments | AGAPLASTIC IND. COM. LTDA. |
| Establishment registrations | 9615834 |
| FEI numbers | 3003080016 |
| Establishment operations | Complaint File Establishment, Foreign Private Label Distributor, Manufacturer |
| 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