Lr Med, Inc. is one of 21901 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lr Med, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ossler Exam Scope
1
Total
1
Cleared
0
Denied
Lr Med, Inc. has 1 FDA 510(k) cleared medical devices. Based in Burr Ridge, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lr Med, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Compliance Consultants as regulatory consultant.
FDA 510(k) Regulatory Record - Lr Med, Inc.
1 devices