Acuson L558 Transducer

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K861579 ↗

FDA Product Code

JOP

Device Class

Class II

Regulation

21 CFR Part 870.2880

Advisory Committee

Cardiovascular

FDA Decision

SN

• Acuson L538 Transducer

  Class II

  FDA 510(k) K871506 Active Cleared 28 Sep 1987

• Acuson S228 and S328 Transducers for Abdom. Appli.

  Class II

  FDA 510(k) K874363 Active Cleared 2 May 1988

• Acuson BL538 Transducer

  Class II

  FDA 510(k) K854786 Active Cleared 15 Jan 1986

• Acuson L382 and L312 Transducers

  Class II

  FDA 510(k) K861866 Active Cleared 18 Jul 1986

• Acuson AL538 Transducer

  Class II

  FDA 510(k) K854788 Active Cleared 15 Jan 1986

• Acuson S328, L382, L538 & L312 Transducers

  Class II

  FDA 510(k) K861578 Active Cleared 17 Jun 1986

See all devices from Acuson Computed Sonography →