Technology Delivery Systems, Inc. is one of 15062 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Technology Delivery Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MAXIFLEX - SEMI FLEX SCOPE, 25 TO 65 CM, MAXIFLEX-SEMI FLEX SCOPE
3
Total
3
Cleared
0
Denied
Technology Delivery Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Pleasant Hill, US.
Historical record: 3 cleared submissions from 2002 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Technology Delivery Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Technology Delivery Systems, Inc.
3 devices