Biomedical Dynamics Disposable Pressure Infusor

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

510(k) Number

K861977 ↗

FDA Product Code

KZD

Device Class

Class I

Regulation

21 CFR Part 880.5420

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Correct Flo Intravascular Administration Set

  Class II

  FDA 510(k) K850506 Active Cleared 1 Apr 1985

• Pressure Infusor for I.V. Bags/Autoinflation

  Class II

  FDA 510(k) K890268 Active Cleared 5 May 1989

• Infusable

  Class I

  FDA 510(k) K911216 Active Cleared 22 Jul 1991

• Pressure Infuser

  Class I

  FDA 510(k) K913751 Active Cleared 9 Jan 1992

• Blood Pressure Cuff

  Class II

  FDA 510(k) K881799 Active Cleared 14 Oct 1988

• Aneroid Blood Pressure Gauge

  Class I

  FDA 510(k) K904376 Active Cleared 20 Dec 1990

See all devices from Biomedical Dynamics, Inc. →