Hemostatix Medical Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hemostatix Medical Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: HEMOSTATIX MODEL P8400 DISPOSABLE HANDLE, HEMOSTATIX MODEL P8400 DISPOSABLE BLADES
2
Total
2
Cleared
0
Denied
Hemostatix Medical Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Bartlett, US.
Historical record: 2 cleared submissions from 2009 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hemostatix Medical Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hemostatix Medical Technologies, LLC
2 devices