FDA 510(k) Applications Submitted by Repro-Med Systems, Inc. dba RMS Medical Products

FDA 510(k) Number Submission Date Device Name Applicant
K122404 08/07/2012 MODEL NUMBER: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604, RMS2-2614, RMS2-2404, RMS2-2414, RMS3-2604, RMS3-26 REPRO-MED SYSTEMS, INC. DBA RMS MEDICAL PRODUCTS
K180843 04/02/2018 HIgH-Flo Super26 Subcutaneous Needle Sets Repro-Med Systems, Inc. dba RMS Medical Products


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