FDA device listing
BACTRACK Element,BACTRACK S75,BACTRACK S78,BACTRACK S80,BACTRACK S82
FDA device listing 1789039957 · DA TECH CO LTD
Key facts
| Proprietary names | BACTRACK Element,BACTRACK S75,BACTRACK S78,BACTRACK S80,BACTRACK S82 |
|---|---|
| Owner/operator | DA TECH CO LTD |
| Owner/operator number | 10027379 |
| Premarket submissions | K090067 |
| Product codes | DJZ |
| Device names | DJZ - Devices, Breath Trapping, Alcohol |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.3050 |
| Review panels | Clinical Toxicology |
| Registered establishments | DA TECH CO LTD |
| Establishment registrations | 3007343307 |
| FEI numbers | 3007343307 |
| Establishment operations | Foreign Exporter, 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