Medical Device Manufacturer · US , New York , NY

Repro-Medical System, Inc., Dba Koru Medical Systems - FDA 510(k) Cle...

2 submissions · 2 cleared · Since 2021
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
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