Donaldson Vent Tube

No FDA recalls found in the data synced 12 Oct 2026.

510(k) Number

K823910 ↗

FDA Product Code

ETD

Device Class

Class II

Regulation

21 CFR Part 874.3880

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Mcgee 26GA. Suction Tube

  Class I

  FDA 510(k) K823437 Active Cleared 9 Dec 1982

• Armstrong V Tube Suction Inserter

  Class I

  FDA 510(k) K822349 Active Cleared 13 Sep 1982

• Vein Graft Ear Scissors

  Class I

  FDA 510(k) K870756 Active Cleared 3 Mar 1987

• Microsurgical Gauge

  Class I

  FDA 510(k) K823436 Active Cleared 9 Dec 1982

• Grommet Vent Tube

  Class II

  FDA 510(k) K823908 Active Cleared 28 Jan 1983

• Universal Speculum Holder

  Class I

  FDA 510(k) K822370 Active Cleared 9 Sep 1982

See all devices from Treace Medical, Inc. →