FDA device listing
Protekt Regulator
FDA device listing 1001166079 · PROACTIVE MEDICAL PRODUCTS LLC
Key facts
| Proprietary names | Protekt Regulator |
|---|---|
| Owner/operator | PROACTIVE MEDICAL PRODUCTS LLC |
| Owner/operator number | 10039097 |
| Product codes | CAN |
| Device names | CAN - Regulator, Pressure, Gas Cylinder |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.2700 |
| Review panels | Anesthesiology |
| Registered establishments | Proactive Medical Products |
| Establishment registrations | 3009327812 |
| FEI numbers | 3009327812 |
| Establishment operations | Complaint File Establishment |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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