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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name thermometer, electronic, clinical
510(K) Number K122221
Model TD-1265
Device Name NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER
Applicant
TAIDOC TECHNOLOGY CORPORATION
3f,5f, no.127, wugong 2nd rd.
wugu district
new taipei city, 
Contact meiru li
Regulation Number880.2910
Classification Product Code
FLL  
Date Received07/25/2012
Decision Date 03/29/2013
Decision substantially equivalent (SE)
Classification Advisory Committee General Hospital
Review Advisory Committee General Hospital
summary summary
Type Special
Reviewed by Third Party No
Expedited Review No
Combination Product No
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