Ssd 5500 with Olympus Gf Type UC140P-AL5

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

510(k) Number

K011315 ↗

FDA Product Code

IYN

Device Class

Class II

Regulation

21 CFR Part 892.1550

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Aloka Ssd-3500 Ultrasound System

  Class II

  FDA 510(k) K023996 Active Cleared 18 Dec 2002

• Aloka Ssd-5500 Diagnostic Ultrasound System

  Class II

  FDA 510(k) K992663 Active Cleared 24 Aug 1999

• Ultrasound Data Analysis System, Model Das-RS1

  Class II

  FDA 510(k) K081843 Active Cleared 15 Jul 2008

• Aloka Ust-5258-5 Diagnostic Ultrasound Transducer

  Class II

  FDA 510(k) K964549 Active Cleared 3 Jun 1997

• Aloka Ssd-4000

  Class II

  FDA 510(k) K003739 Active Cleared 27 Dec 2000

• Aloka Ssd-1000 Diagnostic Ultrasound System, Models Asu-1003, Ust-9121, Ust-9124

  Class II

  FDA 510(k) K020668 Active Cleared 10 Jul 2002

See all devices from Aloka Co., Ltd. →