TEG 6s Hemostasis System Citrated: K, KH, RT, FF Assay Cartridge
Apr 2025
28d
Haemonetics
1
Total
1
Cleared
0
Denied
Haemonetics — FDA 510(k) Submissions
Haemonetics has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Multipurpose For In Vitro Coagulation Studies . Use the specialty filter in the sidebar to narrow results.
1 devices