LIDO ACTIVE — Loredan Biomedical, Inc. (510(k) K871793)
LIDO ACTIVE — Loredan Biomedical, Inc. (510(k) K871793) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: LIDO ACTIVE; Applicant: Loredan Biomedical, Inc.; Clearance track: 510(k).
| Device name | LIDO ACTIVE |
|---|---|
| Applicant | Loredan Biomedical, Inc. |
| Clearance track | 510(k) |
| Submission number | K871793 |
| Decision | Substantially Equivalent |
| Decision date | 1987-06-05 |
| Date received | 1987-05-07 |
| Product code | IKK |
| Device class | 2 |
| Medical specialty | Physical Medicine |
| Applicant location | CA, US |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →