Hemostatix Medical Technologies, LLC is one of 25971 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, MODEL P8400 HEMOSTATIX THERMAL SCALPEL SYSTEM
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hemostatix Medical Technologies, LLC
2 devices