510(k) K103200 ยท FMF Syringe, Piston
PROPEP DELIVERY DEVICE
| Applicant | Rhythmlink International, LLC, Columbia SC, US |
| Decision | Substantially Equivalent, Apr 12, 2011 |
| Received | Nov 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103200
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.