Anthron Catheter Set

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

510(k) Number

K802918 ↗

FDA Product Code

FOZ

Device Class

Class II

Regulation

21 CFR Part 880.5200

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Tube, Leatherman/Imbruce

  Class I

  FDA 510(k) K781665 Active Cleared 15 Dec 1978

• Stethoscope with Temperature Sensor

  Class II

  FDA 510(k) K791190 Active Cleared 6 Jul 1979

• Manipulator & Injector, Uterine

  Class II

  FDA 510(k) K770727 Active Cleared 26 Apr 1977

• Double Lumen Tracheal Tube

  Class II

  FDA 510(k) K802505 Active Cleared 13 Mar 1981

• Reinforced Tracheostomy Tube Set(Tentat)

  Class II

  FDA 510(k) K810321 Active Cleared 4 Mar 1981

• Mlt Tube Microlaryngeal Tracheal Tube)

  Class II

  FDA 510(k) K801005 Active Cleared 23 May 1980

See all devices from National Catheter Co. Div. Mallinckrodt →