Hakki Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hakki Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LotusCatheter (Lotus No Balloon Catheter)
2
Total
1
Cleared
0
Denied
Hakki Medical Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Pinellas Park, US.
Historical record: 1 cleared submissions from 2011 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Hakki Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hakki Medical Technologies, Inc.
2 devices