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 |
|
|