LYK

Angioscope

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)

Last three years. Most recent: 2026-01-28.

NumberDecision dateApplicantDevice nameSummary
K2538422026-01-28Vena Medical Holdings CorpVena MicroAngioscope™ SystemPDF
K2517672025-10-01Vena Medical Holdings CorpVena MicroAngioscope™ SystemPDF

2 summaries are archived here for direct download.

Official FDA classification page: LYK
Classification and pathway per current FDA publications. Data from openFDA (CC0).