Ametek - FDA 510(k) Cleared Devices

Ametek, is a leading global provider of differentiated electronic instruments and electromechanical devices. The company designs and manufactures advanced analytical, test, and measurement solutions for niche markets worldwide, with a manufacturing facility in Largo, US.

AMETEK has received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory focus centers on Neurology devices. The clearance was granted in 2004. As a historical record, AMETEK has not pursued additional FDA 510(k) submissions in recent years.

The company's cleared device portfolio includes dynamometer systems designed for neurological assessment and measurement. AMETEK's strength lies in solving complex technical challenges through niche market focus, operational excellence, and disciplined innovation across its electronic instruments and electromechanical device divisions.

Explore the complete regulatory history, device names, product codes, and clearance dates in the FDA 510(k) database records below.