Therapeutic Apheresis System

No FDA recalls found in the data synced 6 Oct 2026.

Generic Name

Separator, automated, blood cell and plasma, therapeutic

PMA Number

P850092 ↗

FDA Product Code

LKN

Device Class

U

Advisory Committee

Gastroenterology, Urology

FDA Decision

APWD Approval withdrawn

• Millex Vv, Gv, and Hv Syringe Filter Units

  Class II

  FDA 510(k) K023892 Active Cleared 17 Jan 2003

• Waters 740 Data Module-Plotter Integrator

  Class I

  FDA 510(k) K850272 Active Cleared 6 Mar 1985

• Waters(Tm) 996 Pda

  Class I

  FDA 510(k) K924347 Active Cleared 11 Dec 1992

• Light Diagnostics Hsv 1/2 Typing Dfa Kit

  Class II

  FDA 510(k) K081527 Active Cleared 1 Apr 2009

• Ultra-Free

  Class I

  FDA 510(k) K790445 Active Cleared 28 Jun 1979

• Millipore Ivex Int Filter Unit

  Class II

  FDA 510(k) K832952 Active Cleared 4 Oct 1983

See all devices from Millipore Corp. →