Cobe Spectra Blood Component Separator Therapeutic

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K900105 ↗

FDA Product Code

LKN

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Flowmeter, Optiflo Gas

  Class II

  FDA 510(k) K790546 Active Cleared 11 May 1979

• Cobe Ppd 1.9

  Class II

  FDA 510(k) K812336 Active Cleared 31 Aug 1981

• Cobe Emergency Power Source 43610-000

  Class II

  FDA 510(k) K842138 Active Cleared 3 Aug 1984

• Centry 2 Ultrafiltration Control Kit, #018762-002

  Class II

  FDA 510(k) K881062 Active Cleared 21 Apr 1988

• Cobe Rx Meter

  Class II

  FDA 510(k) K830629 Active Cleared 6 Apr 1983

• New Cobe Centrysystem(Tm) 100 Hg Dialyzer

  Class II

  FDA 510(k) K904566 Active Cleared 12 Dec 1990

See all devices from Cobe Laboratories, Inc. →