Shenzhen Viatom Technology Co., Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Shenzhen Viatom Technology Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Shen Zhen, CN.
Latest FDA clearance: Feb 2025. Active since 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Viatom Technology Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Shenzhen Viatom Technology Co., Ltd.
5 devices
Cleared
Feb 28, 2025
Pulse Oximeter ( PO2, PO2A, PO2B)
Anesthesiology
158d
Cleared
Nov 08, 2022
Oxyfit Pulse Oximeter
Anesthesiology
680d
Cleared
Jun 25, 2020
Blood Pressure Monitor
Cardiovascular
205d
Cleared
Dec 02, 2019
Checkme O2 Pulse Oximeter
Anesthesiology
222d
Cleared
Aug 19, 2019
Blood Pressure Monitor
Cardiovascular
196d