Extricare Npwt Foot Dressing

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K131464 ↗

FDA Product Code

OMP

Device Class

Class II

Regulation

21 CFR Part 878.4780

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Devon Accubp Cuff

  Class II

  FDA 510(k) K090664 Active Cleared 23 Mar 2009

• extriCARE 2400 NPWT System with extriCARE 2400 NPWT Pump and extriCARE NPWT Foam Dressing Kit

  Class II

  FDA 510(k) K140634 Active Cleared 19 Sep 2014

• Extricare

  Class II

  FDA 510(k) K132225 Active Cleared 15 May 2014

• Arterioflow Model 7500 Sequential Compression Device

  Class II

  FDA 510(k) K102582 Active Cleared 7 Oct 2010

• Circuflow 5100 Sequential Compression Device

  Class II

  FDA 510(k) K100446 Active Cleared 5 Mar 2010

• Circuflow 5200 Sequential Compression Device

  Class II

  FDA 510(k) K101523 Active Cleared 17 Jun 2010

See all devices from Devon Medical, Inc. →