Nicos (Non-Invasive Cardiac Output System)

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

510(k) Number

K904499 ↗

FDA Product Code

KFG

Device Class

Class I

Regulation

21 CFR Part 866.3040

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Ackrad Endotracheal Tube Introducing Guide

  Class I

  FDA 510(k) K844557 Active Cleared 17 Dec 1984

• Ackrad Bronchitrac

  Class I

  FDA 510(k) K822398 Active Cleared 4 Oct 1982

• Modified Infant Nasal Cannulae Assembly

  Class II

  FDA 510(k) K895031 Active Cleared 30 Oct 1989

• Ackrad Hysterosalpingography Set

  Class II

  FDA 510(k) K842231 Active Cleared 19 Sep 1984

• N-D0-Sure

  Class I

  FDA 510(k) K811185 Active Cleared 2 Jun 1981

• H/S Catheter Set (61-3005, 61-3007, 61-3605, 61-3607)

  Class II

  FDA 510(k) K953034 Active Cleared 29 Aug 1995

See all devices from Ackrad Laboratories →