Midwest Reprocessing Center, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Midwest Reprocessing Center, LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Midwest Reprocessing Center, LLC has 4 FDA 510(k) cleared medical devices. Based in Birmingham, US.
Historical record: 4 cleared submissions from 2010 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Midwest Reprocessing Center, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Midwest Reprocessing Center, LLC
4 devices
Cleared
Jun 08, 2011
MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS
Cardiovascular
58d
Cleared
Oct 07, 2010
MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE
Anesthesiology
154d
Cleared
Aug 27, 2010
MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS,...
Cardiovascular
107d
Cleared
Aug 27, 2010
MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS
Cardiovascular
71d