The first human to live with a fully mechanical heart proved that medicine could replace the organ it had always treated as irreplaceable.

Jarvik-7 Artificial Heart

work concluded confidence: High status: Draft updated 2026-08-11

Type
work
Status
Draft
Confidence
High
Tier
S
Builder-tier
S
Activity-signal
1982-12-02 · https://medicine.utah.edu/sites/g/files/zrelqx356/files/migration/media/first-artificial-heart-anderson.pdf
Activity-checked
2026-08-14
Focus
medical device, artificial organs, cardiovascular surgery, clinical first, mechanical circulatory support
Domain
health-bio
Era
1967–1990 (development); December 2, 1982 (landmark implant)
Primary Location
Salt Lake City, UT
Utah Location
Salt Lake City, UT
Region
Salt Lake City
Website
https://medicine.utah.edu/sites/g/files/zrelqx356/files/migration/media/first-artificial-heart-anderson.pdf
Updated
2026-08-11
Relates
cites DeVries et al. — "Clinical Use of the Total Artificial Heart" (NEJM, 1984) · https://doi.org/10.1056/NEJM198402023100501
Relates
cites U of U Cardiology — Artificial Heart History · https://medicine.utah.edu/sites/g/files/zrelqx356/files/migration/media/first-artificial-heart-anderson.pdf
Relates
cites Smithsonian — Dr. Jarvik Presents Artificial Hearts · https://americanhistory.si.edu/press/releases/dr-jarvik-presents-artificial-hearts-smithsonians-national-museum-american-history

Summary

The Jarvik-7 was a pneumatically driven artificial heart developed by Robert Jarvik under the direction of Willem Kolff at the University of Utah's Division of Artificial Organs. Before the Jarvik-7 implant, replacing the human heart with a machine was theoretical.

Impact

Before the Jarvik-7 implant, replacing the human heart with a machine was theoretical. The Clark operation made it real, and in doing so opened the clinical, regulatory, and engineering path for all subsequent mechanical circulatory support. Ventricular assist devices, the CardioWest Total Artificial Heart (a direct Jarvik-7 descendant), and today's bridge-to-transplant devices are all downstream from the work done in Salt Lake City.

The FDA's experience evaluating the Jarvik-7 trial also helped shape how implantable devices are regulated. Kolff's artificial organs program simultaneously advanced hemodialysis dialysis research; Salt Lake City became the world center of artificial-organ research for decades, a role that seeded the broader Utah medical-device ecosystem.

What It Took

A pneumatically driven artificial heart built from polyurethane and aluminum, sized to fit inside a human chest cavity, and connected to an external air compressor via percutaneous pneumatic lines. The device had two ventricles that alternately inflated and deflated to pump blood through the pulmonary and systemic circulation. Barney Clark's heart was removed; the Jarvik-7 took its place entirely.

The harder engineering problem was not making the pump move but making it move without killing the patient: avoiding hemolysis, managing clotting, surviving infection risk, tolerating indefinite mechanical cycling, and using materials that tissue and blood would not reject over months.

Utah Context

The Jarvik-7 is the canonical example of Utah's artificial-organ tradition. Kolff brought his vision and expertise to the University of Utah from the Netherlands and Cleveland, and built a sustained research program that attracted engineers, physicians, and students who went on to found or lead medical-device companies across the region. The Jarvik-7 is why Salt Lake City had a serious biomedical engineering culture before the broader Utah tech ecosystem formed. The University of Utah's James LeVoy Sorenson Center for Medical Innovation sits inside this lineage.

Evidence

Open Questions

  • The external drive unit was never practical for long-term quality of life; the ethics and framing of the Clark trial remain a live bioethics case study.
  • A fuller account of the animal-experiment program that preceded Clark would strengthen the evidence base.
  • What primary records establish the Jarvik-7's direct relationship to the modern SynCardia device and the regulatory framework it helped establish?