RANDOX EVIDENCE — Randox Laboratories, Ltd. (510(k) K030360)
RANDOX EVIDENCE — Randox Laboratories, Ltd. (510(k) K030360) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: RANDOX EVIDENCE; Applicant: Randox Laboratories, Ltd.; Clearance track: 510(k).
| Device name | RANDOX EVIDENCE |
|---|---|
| Applicant | Randox Laboratories, Ltd. |
| Clearance track | 510(k) |
| Submission number | K030360 |
| Decision | Substantially Equivalent |
| Decision date | 2003-12-23 |
| Date received | 2003-02-03 |
| Product code | DIO |
| Device class | 2 |
| Medical specialty | Clinical Toxicology |
| Applicant location | GB |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →