Home / 510(k) Clearances / K113576

510(k) K113576

DOUBLE LUMEN VIDEO TRACHEOSDOPE (DLVT) SYSTEM by Etview , Ltd. — Product Code CBI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 18, 2012
Date Received
December 5, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
Device Class
Class II
Regulation Number
868.5740
Review Panel
AN
Submission Type

Other clearances by Etview , Ltd.

  • K181880 — VivaSight-SL (TVT) system (November 29, 2018)
  • K181886 — VivaSight-DL System (November 14, 2018)
  • K152438 — ETView VivaSight-SL (TVT) system (February 25, 2016)
  • K123853 — VIVASIGHT-DL SYSTEM (April 15, 2013)
  • K121028 — ETVIEW TRACHEOSCOPIC VENTILATION TUBE (TVT(TM)) (June 21, 2012)
  • K120334 — VIVA EB (June 8, 2012)
  • K082420 — TRACHEOSCOPIC VENTILATION TUBE (TVT) (October 8, 2008)
  • K052233 — TRACHEOSCOPIC VENTILATION TUBE (TVT) SYSTEM (December 13, 2005)

Other clearances for product code CBI

  • K253096 — Chartis Precision Catheter (February 13, 2026)
  • K232529 — Disposable Double Lumen Endobronchial Tube (May 13, 2024)
  • K232580 — Disposable Endobronchial Blocker Tube (December 14, 2023)
  • K222340 — Chartis Precision Catheter (December 1, 2022)
  • K201026 — sOLVe Tube (August 10, 2021)
  • K203749 — Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable (May 3, 2021)
  • K200968 — ABC33L, ABC35L, ABC37L, ABC39L, ABC33R, ABC35R, ABC37R, ABC39R (December 28, 2020)
  • K181886 — VivaSight-DL System (November 14, 2018)
  • K180253 — Sheridan Endobronchial Tubes (November 2, 2018)
  • K160542 — 5.0 Fr Arndt Endobronchial Blocker Set (August 2, 2016)