Dell Corning Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dell Corning Corporation has 1 FDA 510(k) cleared medical devices. Based in Spartanburg, US.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Dell Corning Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dell Corning Asia Co., Ltd. as regulatory consultant.
1 devices