Repro-Med Systems, Inc. Dba Rms Medical Products - FDA 510(k) Cleared...
3
Total
3
Cleared
0
Denied
Repro-Med Systems, Inc. Dba Rms Medical Products has 3 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 3 cleared submissions from 2013 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Repro-Med Systems, Inc. Dba Rms Medical Products Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Repro-Med Systems, Inc. Dba Rms...
3 devices
Cleared
Apr 04, 2019
HIgH-Flo Super26 Subcutaneous Needle Sets
General Hospital
367d
Cleared
Aug 31, 2017
Integrated Catch-up Freedom Syringe Driver Infusion System
General Hospital
346d
Cleared
May 06, 2013
MODEL NUMBER: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604,...
General Hospital
272d