Breathing Filters 1942T/1941T/2014T

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

510(k) Number

K925462 ↗

FDA Product Code

CAH

Device Class

Class II

Regulation

21 CFR Part 868.5260

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Manometer

  Class II

  FDA 510(k) K122077 Active Cleared 10 Jan 2013

• Disposable Gas Sampling Line with and Without in-Line Filter

  Class II

  FDA 510(k) K122075 Active Cleared 20 Dec 2012

• Clear-Therm 3 Hmef, Clear-Therm 3 with Superset Catheter Mount, Clear-Therm with Flexible Catheter Mount, Clear-Guard 3 F3

  Class II

  FDA 510(k) K024270 Active Cleared 24 Jun 2003

• Flo-Guard Breathing Filter

  Class II

  FDA 510(k) K121026 Active Cleared 2 Nov 2012

• Clear-Guard Midi, Clear-Guard Midi W/Flextube, Clear-Therm Mini, Clear-Therm Mini W/Flextube, Models 1644, 1644-T, 1831, 18

  Class II

  FDA 510(k) K983610 Active Cleared 30 Apr 1999

• Intersurgical Inter-Therm Breathing Filter and Heat and Moisture Exchanger, Intersurgical Inter-Guard Breathing Filter

  Class II

  FDA 510(k) K092451 Active Cleared 29 Oct 2010

See all devices from Intersurgical, Inc. →