Dinamap Models 1160 and 1165

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K782073 ↗

FDA Product Code

DSK

Device Class

Class II

Regulation

21 CFR Part 870.1110

Advisory Committee

Cardiovascular

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

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