Procell Surgical, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Procell Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ProCell Surgical Sponge-Blood Recovery Unit
1
Total
1
Cleared
0
Denied
Procell Surgical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Procell Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Procell Surgical, Inc.
1 devices