ClearanceBrief
Company ยท IL

Etview , Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2018. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BTRTube, Tracheal (W/Wo Connector)5
CBITube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)4

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 29, 2018K181880VivaSight-SL (TVT) system
Etview , Ltd., IL
BTR
Nov 14, 2018K181886VivaSight-DL System
Etview , Ltd., IL
CBI
Feb 25, 2016K152438ETView VivaSight-SL (TVT) system
Etview , Ltd., IL
BTR
Apr 15, 2013K123853VIVASIGHT-DL SYSTEM
Etview , Ltd., IL
CBI
Jun 21, 2012K121028ETVIEW TRACHEOSCOPIC VENTILATION TUBE (TVT(TM))
Etview , Ltd., IL
BTR
Jun 8, 2012K120334VIVA EB
Etview , Ltd., IL
CBI
May 18, 2012K113576DOUBLE LUMEN VIDEO TRACHEOSDOPE (DLVT) SYSTEM
Etview , Ltd., IL
CBI
Oct 8, 2008K082420TRACHEOSCOPIC VENTILATION TUBE (TVT)
Etview, IL
BTR
Dec 13, 2005K052233TRACHEOSCOPIC VENTILATION TUBE (TVT) SYSTEM
Etview , Ltd., IL
BTR

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes