Epicor Medical, Inc. is one of 25235 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Epicor Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ULTRACINCH ABLATION DEVICE, ULTRACINCH ACCESSORY PACK, MODELS UC-8, UC-9, UC-10, UC-11, UC-12, UC-13, UC-14, UC-ACC-1, EPICOR MEDICAL ABLATION SYSTEM
2
Total
2
Cleared
0
Denied
Epicor Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Epicor Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Epicor Medical, Inc.
2 devices