Hemostace, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hemostace, LLC - FDA 510(k) Cleared Devices
1
Total
0
Cleared
0
Denied
Hemostace, LLC has 0 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 0 cleared submissions from 1998 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hemostace, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hemostace, LLC
1 devices