Taidoc Technology Corporation - FDA 510(k) Cleared Devices
123
Total
123
Cleared
0
Denied
FDA 510(k) cleared devices by Taidoc Technology Corporation Anesthesiology ✕
5 devices
Cleared
Mar 02, 2016
Finger Type Pulse Oximeter
Anesthesiology
321d
Cleared
Mar 21, 2013
CLEVER TD-7001NEBULIZER
Anesthesiology
251d
Cleared
Feb 28, 2013
U-RIGHT COMPRESSOR NEBULIZER
Anesthesiology
238d
Cleared
Nov 22, 2011
VTRUST FINGER TYPE PULSE OXIMETER
Anesthesiology
237d
Cleared
Dec 15, 2010
V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201
Anesthesiology
247d