Taidoc Technology Corporation - FDA 510(k) Cleared Devices
Recent clearances: XPER Technology PREMIUM Pro Blood Glucose Monitoring System, FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System, Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241)
123
Total
123
Cleared
0
Denied
FDA 510(k) Regulatory Record - 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