Jobst Extremity Pump System 7500

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

Full name

Jobst Extremity Pump(R) System 7500

510(k) Number

K882683 ↗

FDA Product Code

JOW

Device Class

Class II

Regulation

21 CFR Part 870.5800

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Jobst Athrombic Pump - System 2500

  Class II

  FDA 510(k) K934639 Active Cleared 9 Feb 1994

• Jobst Extremity Pump System 7500

  Class II

  FDA 510(k) K921562 Active Cleared 22 Jun 1992

• Comprinet, Comtesse and Bellavar Stockings

  Class II

  FDA 510(k) K905631 Active Cleared 7 Mar 1991

• Ulcercare

  Class II

  FDA 510(k) K892867 Active Cleared 20 Jul 1989

• Yours Truly Asymmetrical Breast Form

  Class I

  FDA 510(k) K911247 Active Cleared 29 Mar 1991

• Anti-Em/Gp Stockings

  Class II

  FDA 510(k) K955138 Active Cleared 13 Dec 1995

See all devices from Jobst Institute, Inc. →

• What is the Jobst Extremity Pump 7500 used for?

  The Jobst Extremity Pump 7500 is designed for sequential compression therapy. It applies graduated pressure to an extremity through a three-chambered sleeve to promote venous return and help manage conditions like chronic venous insufficiency or lymphedema. The device mimics natural muscle contractions to encourage circulation and reduce edema.

• Is the Jobst Extremity Pump 7500 reusable or single-use?

  The Jobst Extremity Pump 7500 is a reusable medical device. It requires connection to an external power source for operation and is intended for repeated use across multiple patients, provided it is properly cleaned and maintained between uses.

• What sleeve sizes are available for the Jobst Extremity Pump 7500?

  The Jobst Extremity Pump 7500 is compatible with multiple sleeve sizes to accommodate different limb applications. While the exact sizes are not listed in the specifications, the device is designed to fit a range of extremities, including arms and legs, for effective compression therapy.

• How is the pressure adjusted on the Jobst Extremity Pump 7500?

  The Jobst Extremity Pump 7500 includes an adjustable pressure gauge, allowing clinicians to customize the compression levels based on patient needs. This feature ensures the device can be tailored for different therapeutic requirements, such as mild or moderate edema management.

• What regulatory pathway does the Jobst Extremity Pump 7500 follow?

  The Jobst Extremity Pump 7500 holds FDA 510(k) clearance (K882683) under the Traditional pathway. It is classified as a Class II device under FDA regulations (870.5800), indicating it has undergone review by the FDA’s Cardiovascular (CV) advisory committee to ensure safety and effectiveness for sequential compression therapy.