Ymed, Inc. is one of 25095 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ymed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VASCUTRAK 2, MODELS: V14 AND V18, VASCUTRAK PTA DILATION CATHETER
2
Total
2
Cleared
0
Denied
Ymed, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 2006 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ymed, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ymed, Inc.
2 devices