FDA device listing
BREAKAWAY LAP CUSHION,DROP SEAT,EXTENDED-WIDTH ARMREST,FOOTREST ELEVATION KIT,INFLATABLE LAP BUDDY,O2 TANK HOLDER,PADDED…
FDA device listing 1515420860 · ALIMED, LLC
Key facts
| Proprietary names | BREAKAWAY LAP CUSHION,DROP SEAT,EXTENDED-WIDTH ARMREST,FOOTREST ELEVATION KIT,INFLATABLE LAP BUDDY,O2 TANK HOLDER,PADDED HEAD SUPPORTS,PREMIER WHEELCHAIR ARM TRAY,PUSH CUFF,RESTRAINT-FREE CUSHIONED LAP BELT,UNILOOP,WHEELCHAIR FOOT SUPPORT,WHEELCHAIR SIDE SUPPORTS |
|---|---|
| Owner/operator | ALIMED, LLC |
| Owner/operator number | 1218386 |
| Product codes | KNO |
| Device names | KNO - Accessories, Wheelchair |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3910 |
| Review panels | Physical Medicine |
| Registered establishments | ALIMED, LLC |
| Establishment registrations | 1218386 |
| FEI numbers | 1218386 |
| Establishment operations | Manufacturer, Specification Developer |
| 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