Konsyl Pharmaceuticals is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Konsyl Pharmaceuticals - FDA 510(k) Cleared Devices
Recent clearances: SITZMARKS
1
Total
1
Cleared
0
Denied
Konsyl Pharmaceuticals has 1 FDA 510(k) cleared medical devices. Based in Easton, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Konsyl Pharmaceuticals Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Prism Medical Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Konsyl Pharmaceuticals
1 devices