FDA device listing
Air transfer mattress;disposable air transfer mattress,mattress,Mattress, Flotation Therapy, Non-Powered,reusable air…
FDA device listing 1901427155 · YEARSTAR HEALTHCARE TECHNOLOGY CO., LTD.
Key facts
| Proprietary names | Air transfer mattress;disposable air transfer mattress,mattress,Mattress, Flotation Therapy, Non-Powered,reusable air transfer mattress,air assisted transfer mattress |
|---|---|
| Owner/operator | YEARSTAR HEALTHCARE TECHNOLOGY CO., LTD. |
| Owner/operator number | 10080151 |
| 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 | YEARSTAR HEALTHCARE TECHNOLOGY CO.,LTD |
| Establishment registrations | 3018269545 |
| FEI numbers | 3018269545 |
| Establishment operations | Contract Manufacturer, 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