Sterilmed Inc. (Johnson and Johnson) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sterilmed Inc. (Johnson and Johnson) - FDA 510(k) Cleared Devices
Recent clearances: Reprocessed PentaRay Nav eco High-Density Mapping Catheter
1
Total
1
Cleared
0
Denied
Sterilmed Inc. (Johnson and Johnson) has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sterilmed Inc. (Johnson and Johnson) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sterilmed Inc. (Johnson and Johnson)
1 devices