Vacon Tm

No FDA recalls on record, checked 12 Oct 2026.

510(k) Number

K770369 ↗

FDA Product Code

CBD

Device Class

Class II

Regulation

21 CFR Part 880.6740

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Cuff-Mate 2 Endotracheal Cuff Inflator & Monitor

  Class II

  FDA 510(k) K902114 Active Cleared 18 Jul 1990

• Medshield/Aerochamber

  Class I

  FDA 510(k) K961455 Active Cleared 25 Jul 1996

• Respirex 2

  Class II

  FDA 510(k) K900754 Active Cleared 15 Mar 1990

• O2 Connector

  Class I

  FDA 510(k) K780750 Active Cleared 27 Jul 1978

• Therapep W/Mouthpiece, W/Pediatric Mask, W/Small Mask, W/Large Mask, Resistor/Port/Mouthpiece, Resistor/Port

  Class II

  FDA 510(k) K962749 Active Cleared 10 Oct 1996

• Filter, Vacuum Line Lineguard

  Class II

  FDA 510(k) K760420 Active Cleared 23 Aug 1976

See all devices from Diemolding Corp. →