A.B. Korkor Medical, Inc. is one of 24658 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A.B. Korkor Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH
1
Total
1
Cleared
0
Denied
A.B. Korkor Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in North Barrington, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by A.B. Korkor Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - A.B. Korkor Medical, Inc.
1 devices