Clearmedical/Nellcor Oxisensor II, Neonatal/Adult, Model N-25

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K012609 ↗

FDA Product Code

NLF

Device Class

Class II

Regulation

21 CFR Part 870.2700

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Clearmedical/Critikon Blood Pressure Cuff; Clearmedical/Welch Allyn Blood Pressure Cuff

  Class II

  FDA 510(k) K031416 Active Cleared 15 Jul 2003

• Reprocessed Surgical Scissors and Graspers

  Class II

  FDA 510(k) K033592 Active Cleared 27 Jul 2004

• Clearmedical/Huntleigh Foot Garments; Models FG200/Lrg (Large), FG200/Std (Standard), FG100/Sm (Small), FG100-R (Regular

  Class II

  FDA 510(k) K012616 Active Cleared 6 Feb 2002

• Reprocessed Trocars

  Class I

  FDA 510(k) K033591 Active Cleared 3 Jun 2005

• Reloadable Cutters, Staplers, and Appliers, Reprocessed

  Class II

  FDA 510(k) K033578 Active Cleared 11 Jul 2005

• Reprocessed Multiple Clip Appliers

  Class II

  FDA 510(k) K033579 Active Cleared 11 Jul 2005

See all devices from Clearmedical, Inc. →