Honeywell, Inc. - FDA 510(k) Cleared Devices

Honeywell, Inc. is an American multinational conglomerate headquartered in Charlotte, North Carolina. The company operates across aerospace, building automation, industrial automation, and energy solutions.

Honeywell's medical device regulatory history spans from 1976 to 1990. The company received 69 FDA 510(k) clearances from 69 total submissions. Cardiovascular devices represented the dominant focus, accounting for approximately 75% of submissions. This historical record reflects the company's past involvement in patient monitoring systems, defibrillators, and related cardiovascular instrumentation.

The company is now inactive in the medical device regulatory space, with no clearances recorded since 1990. This profile serves as a historical record of Honeywell's contributions to FDA-regulated medical devices during its active period in this sector.

Explore the complete clearance history, including device names, product codes, and specific clearance dates, in the database records below.