FDA device listing
AIR FLOTATION MATTRESS ALTERNATING PRESSURE
FDA device listing 1443337506 · BLUE CHIP MEDICAL PRODUCTS, INC.
Key facts
| Proprietary names | AIR FLOTATION MATTRESS ALTERNATING PRESSURE |
|---|---|
| Owner/operator | BLUE CHIP MEDICAL PRODUCTS, INC. |
| Owner/operator number | 9042507 |
| Product codes | FNM |
| Device names | FNM - Mattress, Air Flotation, Alternating Pressure |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5550 |
| Review panels | General Hospital |
| Registered establishments | BLUE CHIP MEDICAL PRODUCTS, INC. |
| Establishment registrations | 2438690 |
| FEI numbers | 3000299121 |
| Establishment operations | 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