Endoscopic Surgical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endoscopic Surgical Products, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Endoscopic Surgical Products, Inc. has 2 FDA 510(k) cleared medical devices. Based in Minnetonka, US.
Historical record: 2 cleared submissions from 1992 to 1994. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Endoscopic Surgical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Endoscopic Surgical Products, Inc.
2 devices