Neoguide Systems, Inc. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neoguide Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NEOGUIDE ENDOSCOPY SYSTEM, NAVIGATOR ENDOSCOPY SYSTEM
2
Total
2
Cleared
0
Denied
Neoguide Systems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Gatos, US.
Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Neoguide Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neoguide Systems, Inc.
2 devices