Porous Media DBF23 Reusable Respiratory Filter

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K965020 ↗

FDA Product Code

CAH

Device Class

Class II

Regulation

21 CFR Part 868.5260

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Porous Media DPB30 Series Disposable Pre-Bypass Filter

  Class II

  FDA 510(k) K990276 Active Cleared 1 Oct 1999

• Porous Media DBF23 Disposable Respiratory Filter

  Class II

  FDA 510(k) K964979 Active Cleared 11 Mar 1997

• Porous Media DEF25 Disposable Respiratory Filter

  Class II

  FDA 510(k) K982127 Active Cleared 23 Jun 1998

• Porous Media DBF23-R Reusable Respiratory Filter

  Class II

  FDA 510(k) K952428 Active Cleared 7 Jul 1995

• Oxygen Concentrator Filters, Models DBF32, DBF24, DBF27, DBF25, DFC06 and DDF47

  Class II

  FDA 510(k) K061426 Active Cleared 5 Jun 2006

• Porous Media Humidiflow Humidifier for Universal Humidification

  Class II

  FDA 510(k) K062091 Active Cleared 8 Aug 2006

See all devices from Porous Media Corp. →