Christie Medical Holdings, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Christie Medical Holdings, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Presygen/si-1
1
Total
1
Cleared
0
Denied
Christie Medical Holdings, Inc. has 1 FDA 510(k) cleared medical devices. Based in Memphis, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Christie Medical Holdings, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mandell Horwitz Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Christie Medical Holdings, Inc.
1 devices