Cerebral Function Monitor 870

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

510(k) Number

K791580 ↗

FDA Product Code

OMA

Device Class

Class II

Regulation

21 CFR Part 882.1400

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Model 1051, Monitor

  Class II

  FDA 510(k) K790328 Active Cleared 2 Mar 1979

• Dinamap Model 846

  Class II

  FDA 510(k) K781053 Active Cleared 7 Sep 1978

• Model 902 Stand

  Class I

  FDA 510(k) K780759 Active Cleared 19 May 1978

• Electrode, Needle, Cfm

  Class II

  FDA 510(k) K781311 Active Cleared 21 Aug 1978

• Dinamap Model 855

  Class II

  FDA 510(k) K791159 Active Cleared 30 Jul 1979

• Dinamap Model 848

  Class II

  FDA 510(k) K781064 Active Cleared 7 Sep 1978

See all devices from Applied Medical Research →