Hp 77025A/77030A Ultra. System/Hp 77020CV Upgrade

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

510(k) Number

K883481 ↗

FDA Product Code

IYO

Device Class

Class II

Regulation

21 CFR Part 892.1560

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Luer Lock Skirt

  Class II

  FDA 510(k) K862451 Active Cleared 31 Oct 1986

• Hp Sonos 100 Cf Ultrasound Imaging System

  Class II

  FDA 510(k) K922184 Active Cleared 30 Jul 1992

• Medical Diag. Ultrasound Instr. 77065

  Class II

  FDA 510(k) K842897 Active Cleared 25 Sep 1984

• Model M1403A Telemetry Monitoring Systems (TMS)

  Class II

  FDA 510(k) K913533 Active Cleared 7 Nov 1991

• Differential Refractive Index Detector

  Class I

  FDA 510(k) K800556 Active Cleared 25 Mar 1980

• Model 80100A, Patient Data Memory

  Class II

  FDA 510(k) K781360 Active Cleared 7 Sep 1978

See all devices from Hewlett-Packard Co. →

• What is the HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE?

  It is an ultrasonic imaging system classified as a System, Imaging, Pulsed Echo, Ultrasonic, designed for medical imaging applications.

• How is the device supplied?

  The device is supplied as a system upgrade intended for use in clinical settings.

• Is the device intended for single-use or reuse?

  The device is not specified as single-use or reusable.

• What are the specifications for this device?

  The device is classified as a System, Imaging, Pulsed Echo, Ultrasonic and is designed for medical imaging applications.