FDA device listing
Nuocande Plastic Manual Wheelchair Model NKD L07
FDA device listing 1592502868 · Ningbo Lecount Medical Technology Development Co., Ltd.
Key facts
| Proprietary names | Nuocande Plastic Manual Wheelchair Model NKD L07 |
|---|---|
| Owner/operator | Ningbo Lecount Medical Technology Development Co., Ltd. |
| Owner/operator number | 10050382 |
| Premarket submissions | K151797 |
| Product codes | IOR |
| Device names | IOR - Wheelchair, Mechanical |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3850 |
| Review panels | Physical Medicine |
| Registered establishments | NINGBO LECOUNT MEDICAL TECHNOLOGY DEVELOPMENT CO., LTD. |
| Establishment registrations | 3011889389 |
| FEI numbers | 3011889389 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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