510(k) K163233 ยท DQY Catheter, Percutaneous
MIVI 6F 25cm Mi-EXT Extension Catheter, MIVI 5F 25cm Mi-EXT Extension Catheter, MIVI 4F 30cm Mi-EXT Extension Catheter, MIVI 3F 43cm Mi-EXT Extension Catheter
| Applicant | Mivi Neuroscience, Inc., Eden Prarie MN, US |
| Decision | Substantially Equivalent, Apr 6, 2017 |
| Received | Nov 17, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163233
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.