Amptron Medical, Inc. is one of 16268 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amptron Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ElintMAX Respiratory Monitor (ElintMAX Monitor A1)
1
Total
1
Cleared
0
Denied
Amptron Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Amptron Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Amptron Medical, Inc.
1 devices