Cantel is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cantel - FDA 510(k) Cleared Devices
Recent clearances: EON Portable Reverse Osmosis Water Purification System
1
Total
1
Cleared
0
Denied
Cantel has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cantel Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cantel
1 devices