FDA device listing
Accumax,Centrella,Centrella Surface,Compella,Dynamo Series Stretchers,NP100,NP50,Progressa,Progressa+,Stretcher Mattress
FDA device listing 1789577710 · BAXTER HEALTHCARE CORPORATION
Key facts
| Proprietary names | Accumax,Centrella,Centrella Surface,Compella,Dynamo Series Stretchers,NP100,NP50,Progressa,Progressa+,Stretcher Mattress |
|---|---|
| Owner/operator | BAXTER HEALTHCARE CORPORATION |
| Owner/operator number | 1417572 |
| Product codes | IKY |
| Device names | IKY - Mattress, Flotation Therapy, Non-Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5150 |
| Review panels | General Hospital |
| Registered establishments | HILL-ROM DE MEXICO S DE RL DE CV, HILL-ROM, INC. |
| Establishment registrations | 1824206, 3006697241 |
| FEI numbers | 1824206, 3006697241 |
| Establishment operations | Complaint File Establishment, Manufacturer, Repackager/Relabeler, Specification Developer, Contract Manufacturer |
| 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