Century Series Holter Scanner System, Models C3000, C2000 and C1000

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

510(k) Number

K024323 ↗

FDA Product Code

MLO

Models / Variants

C3000

C2000

C1000

Device Class

Class II

Regulation

21 CFR Part 870.2800

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Nurite II Vrm Dual (Elec. Nerve Stim.)

  Class II

  FDA 510(k) K791834 Active Cleared 2 Oct 1979

• Truvue Wireless Ambulatory ECG Monitoring System

  Class II

  FDA 510(k) K100155 Active Cleared 20 Apr 2010

• Nurite II, Single

  Class II

  FDA 510(k) K781683 Active Cleared 13 Oct 1978

• Century Color Trace

  Class II

  FDA 510(k) K884152 Active Cleared 15 Dec 1988

• Nurite II Vrm Single (Elec. Nerve Stim)

  Class II

  FDA 510(k) K791833 Active Cleared 2 Oct 1979

• Nurite II

  Class II

  FDA 510(k) K780828 Active Cleared 31 May 1978