Repro-Med Systems, Inc. Dba Rms Medical Products is one of 18404 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Repro-Med Systems, Inc. Dba Rms Medical Products - FDA 510(k) Cleared...
Recent clearances: HIgH-Flo Super26 Subcutaneous Needle Sets, Integrated Catch-up Freedom Syringe Driver Infusion System, MODEL NUMBER: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604, RMS2-2614, RMS2-2404, RMS2-2414, RMS3-2604, RMS3-26
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) Regulatory Record - Repro-Med Systems, Inc. Dba Rms Medical Products
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