510(k) K171505 ยท FIE Needle, Fistula
Dimesol Disposable AV Fistula Needle Set (Non-Safety Series) and Dimesol Disposable AV Fistula Needle Set (Safety Series)
| Applicant | Dimesol, Inc., Lewisberry PA, US |
| Decision | Substantially Equivalent, May 17, 2018 |
| Received | May 23, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171505
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.