Ametek, Inc. is one of 13059 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ametek, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GASEOUS OXYGEN ANALYZER (MODEL S-3A) MODIFICATION
2
Total
2
Cleared
0
Denied
Ametek, Inc. is a global provider of electronic instruments and electromechanical devices. The company operates with a manufacturing facility in Pittsburgh, US. Ametek serves niche markets through advanced analytical and test measurement solutions.
Ametek has received 2 FDA 510(k) clearances from 2 total submissions. The company's regulatory focus centers on Anesthesiology devices, representing 100% of submissions. Clearances span from 1995 to 1996. Ametek is currently inactive in FDA submissions, with no clearances recorded in more than five years. This profile represents a historical regulatory record.
Historical cleared devices include gaseous oxygen analyzers and carbon dioxide analyzers for anesthesiology applications. These instruments reflect the company's specialization in respiratory gas monitoring technologies for clinical use.
Explore the complete device names, product codes, and clearance dates in the full regulatory database record.
FDA 510(k) Regulatory Record - Ametek, Inc.
2 devices