LYK
- Product code
- LYK
- Device name
- Angioscope
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 2
- Summaries archived here
- 2 (direct download)
- 510(k) clearances (all years, FDA)
- 41 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K253842 | 2026-01-28 | Vena Medical Holdings Corp | Vena MicroAngioscope System | |
| K251767 | 2025-10-01 | Vena Medical Holdings Corp | Vena MicroAngioscope System |
Official FDA classification page: LYK
Classification and pathway per current FDA publications. Data from openFDA (CC0).