510(k) K102512 ยท FPA Set, Administration, Intravascular
RMS SUBCUTANEOUS NEEDLE SET
| Applicant | Repro-Med Systems, Inc., New York NY, US |
| Decision | Substantially Equivalent, May 20, 2011 |
| Received | Sep 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102512
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.