Tandem Medical, Inc. is one of 8461 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tandem Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10, AUTODOSE INFUSION SYSTEM
2
Total
2
Cleared
0
Denied
Tandem Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 1999 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tandem Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tandem Medical, Inc.
2 devices