KZA
6 FDA 510(k) clearances · Product code
140 daysmedian time to decision
232 days90th percentile
6clearances measured
FDA profile
- Official device name
- Device, Vein Location, Liquid Crystal
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6970
- Medical specialty
- General Hospital
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| IV-eye (K152088) | Novarix Limited | 2016-02-24 |
| VTS1000 (K101838) | Vuetek Scientific, LLC | 2011-02-18 |
| IR VIEWER (K042679) | Infrared Imaging Systems, Inc. | 2004-12-10 |
| ESP7 VENOUS IMAGE (K982612) | Ironmaster, Inc. | 1998-12-14 |
| HYPO-GRIP (K780884) | Harco Products | 1978-08-10 |
| E-Z-JECTOR (K780883) | Harco Products | 1978-08-10 |
Track KZA automatically
Every clearance here is in the API, with alerts when new ones post.