FDA device listing
KYX/ DISPENSER, LIQUID MEDICATION
FDA device listing 1198579657 · SMART TECHNOLOGY CO LTD
Key facts
| Proprietary names | KYX/ DISPENSER, LIQUID MEDICATION |
|---|---|
| Owner/operator | SMART TECHNOLOGY CO LTD |
| Owner/operator number | 10051751 |
| Product codes | KYX |
| Device names | KYX - Dispenser, Liquid Medication |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6430 |
| Review panels | General Hospital |
| Registered establishments | Smart Technology Co., Ltd. |
| Establishment registrations | 3012416077 |
| FEI numbers | 3012416077 |
| 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