Compression Works, LLC is one of 5147 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Compression Works, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Compression Works, LLC has 2 FDA 510(k) cleared medical devices. Based in Providence, US.
Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Compression Works, LLC Filter by specialty or product code using the sidebar.
Compression Works, LLC — FDA 510(k) Products and Clearance History
2 devices
Cleared
Dec 06, 2013
ABDOMINAL AORTIC AND JUNCTIONAL TOURNIQUET (AAJT) DEVICE
Cardiovascular
71d
Cleared
Oct 18, 2011
ABDOMINAL TOURNIQUET SYSTEM
Cardiovascular
61d