Medilog 9000-Ii Ambulatory Recorder

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K890647 ↗

FDA Product Code

DSH

Device Class

Class II

Regulation

21 CFR Part 870.2800

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Medilog 2500 System

  Class II

  FDA 510(k) K860078 Active Cleared 26 Feb 1986

• Model 5000 Ambulatory Monitoring System

  Class II

  FDA 510(k) K871500 Active Cleared 1 Jul 1987

• Medilog M6

  Class II

  FDA 510(k) K852892 Active Cleared 9 Dec 1985

• Model Mr-30 Holter Recorder

  Class II

  FDA 510(k) K860181 Active Cleared 26 Feb 1986

• Model 1010 Ambulatory Ph Monitoring System

  Class I

  FDA 510(k) K862536 Active Cleared 12 Sep 1986

• Oxford Intensive Care Patient Mon. Sys

  Class II

  FDA 510(k) K802033 Active Cleared 26 Sep 1980

See all devices from Oxford Medilog, Inc. →