510(k) K183353 ยท DQY Catheter, Percutaneous
Telescope Guide Extension Catheter
| Applicant | Medtronic, Inc., Galway, IE |
| Decision | Substantially Equivalent, Mar 22, 2019 |
| Received | Dec 3, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183353
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.