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Etview , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K181880VivaSight-SL (TVT) systemNovember 29, 2018
K181886VivaSight-DL SystemNovember 14, 2018
K152438ETView VivaSight-SL (TVT) systemFebruary 25, 2016
K123853VIVASIGHT-DL SYSTEMApril 15, 2013
K121028ETVIEW TRACHEOSCOPIC VENTILATION TUBE (TVT(TM))June 21, 2012
K120334VIVA EBJune 8, 2012
K113576DOUBLE LUMEN VIDEO TRACHEOSDOPE (DLVT) SYSTEMMay 18, 2012
K082420TRACHEOSCOPIC VENTILATION TUBE (TVT)October 8, 2008
K052233TRACHEOSCOPIC VENTILATION TUBE (TVT) SYSTEMDecember 13, 2005