FDA device listing
System, Thermal Regulating
FDA device listing 1754844869 · Ag Marketing & Development Group Inc Dba Agmd Group
Key facts
| Owner/operator | Ag Marketing & Development Group Inc Dba Agmd Group |
|---|---|
| Owner/operator number | 10089735 |
| Product codes | DWJ |
| Device names | DWJ - System, Thermal Regulating |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.5900 |
| Review panels | Cardiovascular |
| Registered establishments | AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP |
| Establishment registrations | 3016844398 |
| FEI numbers | 3016844398 |
| Establishment operations | Foreign Private Label Distributor |
| 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