Luer, Jackson Trachea Tubes, Luer Speaking Trachea Tubes

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K953368 ↗

FDA Product Code

BTR

Device Class

Class II

Regulation

21 CFR Part 868.5730

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Trocars, Cannulae, Sheaths, Obturators

  Class II

  FDA 510(k) K943697 Active Cleared 14 Sep 1994

• KSEA Vaporization Electrodes

  Class II

  FDA 510(k) K961702 Active Cleared 29 Aug 1996

• Trocars, Cannulae, Sheaths

  Class II

  FDA 510(k) K943816 Active Cleared 24 Aug 1994

• Ksea Instrument Set for Saphenous Vein Harvesting

  Class II

  FDA 510(k) K973068 Active Cleared 7 Nov 1997

• Ksea Semm Tissur Punch

  Class II

  FDA 510(k) K943053 Active Cleared 21 Mar 1995

• Cholangiography Set

  Class II

  FDA 510(k) K943435 Active Cleared 7 Nov 1994

See all devices from Karl Storz Endoskop GmbH →