Kck Industries is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kck Industries - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kck Industries has 1 FDA 510(k) cleared medical devices. Based in Woodland Hills, US.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kck Industries Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kck Industries
1 devices