Huntleigh Flowpac FP2000

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

510(k) Number

K871272 ↗

FDA Product Code

DRM

Device Class

Class II

Regulation

21 CFR Part 870.5200

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Huntleigh Dynamic Flotation System

  Class II

  FDA 510(k) K890012 Active Cleared 29 Mar 1989

• Huntleigh Double Bubble Air-O-Pad-AOP5

  Class II

  FDA 510(k) K882644 Active Cleared 10 Aug 1988

• Dopcord Ppg

  Class II

  FDA 510(k) K884451 Active Cleared 12 Jan 1989

• Multi Dopplex, Md-1

  Class II

  FDA 510(k) K900882 Active Cleared 22 Aug 1990

• Rheo Dopplex II (Rd 2)

  Class II

  FDA 510(k) K964699 Active Cleared 21 Feb 1997

• Huntleigh Flowpress AC300 Pump, SQ301/302/320 GAR

  Class II

  FDA 510(k) K871271 Active Cleared 15 Sep 1987

See all devices from Huntleigh Technology, Inc. →