FDA device listing
KFT-01 KFT-02 KFT-03 KFT-03C KFT-04 KFT-05 KFT-05L KFT-06 KFT-07 KFT-08 KFT-09 KFT-10 KFT-11 KFT-12 KFT-13 KFT-14…
FDA device listing 1159599801 · Kangfu Medical Equipment Factory
Key facts
| Proprietary names | KFT-01 KFT-02 KFT-03 KFT-03C KFT-04 KFT-05 KFT-05L KFT-06 KFT-07 KFT-08 KFT-09 KFT-10 KFT-11 KFT-12 KFT-13 KFT-14 KFT-15,KFT-16 KFT-17 KFT-18 KFT-22 KFT-22M KFT-23 KFT- 24 KFT-25 KFT-26 KFT-27 KFT-28 |
|---|---|
| Owner/operator | Kangfu Medical Equipment Factory |
| Owner/operator number | 10059139 |
| Product codes | SDV |
| Device names | SDV - Clinical Electronic Thermometer |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.2910 |
| Review panels | General Hospital |
| Registered establishments | KANGFU MEDICAL EQUIPMENT FACTORY |
| Establishment registrations | 3015140207 |
| FEI numbers | 3015140207 |
| 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