Vesatek, LLC

Vesatek, LLC holds 2 FDA 510(k) medical device clearances, first cleared 2017, most recent 2020.

Top product codes for Vesatek, LLC

DQX — Cardiovascular2 devices

Recent clearances by Vesatek, LLC

K200120 — LiteSaber Wire Torque Assist DeviceCode DQX·2020-05-07
K170684 — Firebow Wire Torque Assist DeviceCode DQX·2017-06-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.