Egnell Universal Suction Pump

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

510(k) Number

K853909 ↗

FDA Product Code

BTA

Device Class

Class II

Regulation

21 CFR Part 878.4780

Advisory Committee

General, Plastic Surgery

FDA Decision

SN

• Ameda Neonatal Resuscitation Unit-

  Class II

  FDA 510(k) K832637 Active Cleared 22 Dec 1983

• Ametherm

  Class II

  FDA 510(k) K840526 Active Cleared 30 Apr 1984

• Egnell-Lact B Battery-Operated Breast Pump

  Class II

  FDA 510(k) K844307 Active Cleared 4 Feb 1985

• Egnell Compact, Type Ehv

  Class II

  FDA 510(k) K812020 Active Cleared 20 Oct 1981

• Pe-01 Electronic Infusion Pump

  Class II

  FDA 510(k) K812898 Active Cleared 2 Dec 1981

• Gastric Juices Suction Pump

  Class II

  FDA 510(k) K813095 Active Cleared 9 Dec 1981

See all devices from Egnell, Inc. →