Km Corp. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Km Corp. - FDA 510(k) Cleared Devices
Recent clearances: Perpak™ Sterilization Tyvek Pouch
1
Total
1
Cleared
0
Denied
Km Corp. has 1 FDA 510(k) cleared medical devices. Based in Gangwon-Do, KR.
Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Km Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Km Corp.
1 devices