Etview , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Etview , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: VivaSight-SL (TVT) system, VivaSight-DL System
8
Total
8
Cleared
0
Denied
Etview , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Binyamina, IL.
Historical record: 8 cleared submissions from 2005 to 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Etview , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qsite as regulatory consultant.
FDA 510(k) Regulatory Record - Etview , Ltd.
8 devices
Cleared
Nov 29, 2018
VivaSight-SL (TVT) system
Anesthesiology
139d
Cleared
Nov 14, 2018
VivaSight-DL System
Anesthesiology
124d
Cleared
Feb 25, 2016
ETView VivaSight-SL (TVT) system
Anesthesiology
182d
Cleared
Apr 15, 2013
VIVASIGHT-DL SYSTEM
Anesthesiology
122d
Cleared
Jun 21, 2012
ETVIEW TRACHEOSCOPIC VENTILATION TUBE (TVT(TM))
Anesthesiology
77d
Cleared
Jun 08, 2012
VIVA EB
Anesthesiology
126d
Cleared
May 18, 2012
DOUBLE LUMEN VIDEO TRACHEOSDOPE (DLVT) SYSTEM
Anesthesiology
165d
Cleared
Dec 13, 2005
TRACHEOSCOPIC VENTILATION TUBE (TVT) SYSTEM
Anesthesiology
118d