Last synced on 16 May 2025 at 11:05 pm

MODEL NUMBER: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604, RMS2-2614, RMS2-2404, RMS2-2414, RMS3-2604, RMS3-26

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122404
510(k) Type
Traditional
Applicant
REPRO-MED SYSTEMS, INC. DBA RMS MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2013
Days to Decision
272 days
Submission Type
Summary

MODEL NUMBER: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604, RMS2-2614, RMS2-2404, RMS2-2414, RMS3-2604, RMS3-26

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122404
510(k) Type
Traditional
Applicant
REPRO-MED SYSTEMS, INC. DBA RMS MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2013
Days to Decision
272 days
Submission Type
Summary