Hewlett-Packard Co. - FDA 510(k) Cleared Devices

Hewlett-Packard, Co. is a technology company headquartered in McHenry, US. The company historically developed medical devices alongside its core computing and printing business.

Hewlett-Packard received 229 FDA 510(k) clearances from 230 total submissions, with clearances spanning 1976 to 2000. The company specialized in cardiovascular devices, including defibrillators, telemetry systems, and clinical information systems. Additional cleared devices covered gastroenterology, urology, and radiology applications. This regulatory record reflects the company's historical involvement in patient monitoring and diagnostic technologies.

The company is inactive in the medical device space, with no FDA 510(k) clearances recorded in more than two decades. This profile serves as a historical regulatory record only.

Explore the complete list of device names, product codes, and clearance dates in the database to review Hewlett-Packard's full FDA 510(k) submission history.