FDA device listing
FORA Test N'GO Advance Lactate Test System,heartscare C1 lactate,heartscare C1 monitoring system,L1 Lactate Monitoring…
FDA device listing 1298300014 · TAIDOC TECHNOLOGY CORPORATION
Key facts
| Proprietary names | FORA Test N'GO Advance Lactate Test System,heartscare C1 lactate,heartscare C1 monitoring system,L1 Lactate Monitoring System |
|---|---|
| Owner/operator | TAIDOC TECHNOLOGY CORPORATION |
| Owner/operator number | 9058384 |
| Product codes | KHP |
| Device names | KHP - Acid, Lactic, Enzymatic Method |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1450 |
| Review panels | Clinical Chemistry |
| Registered establishments | TAIDOC TECHNOLOGY CORPORATION |
| Establishment registrations | 3004145393 |
| FEI numbers | 3004145393 |
| 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