Libramedical, Inc. is one of 18426 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Libramedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FlexSeal Introducer Sheath with Hydrophilic Coating
1
Total
1
Cleared
0
Denied
Libramedical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Libramedical, 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 - Libramedical, Inc.
1 devices