Repro-Medical System, Inc., Dba Koru Medical Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Repro-Medical System, Inc., Dba Koru Medical Systems - FDA 510(k) Cle...
Recent clearances: FreedomEdge Syringe Infusion System, FreedomEdge(R) Syringe Infusion System
2
Total
2
Cleared
0
Denied
Repro-Medical System, Inc., Dba Koru Medical Systems has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2022. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Repro-Medical System, Inc., Dba Koru Medical Systems Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by 510K Technology Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Repro-Medical System, Inc., Dba Koru Medical Systems
2 devices