510(k) K190167 ยท DRA Catheter, Steerable
MitraClip G4 Steerable Guide Catheter
| Applicant | Abbott, Santa Clara CA, US |
| Decision | Substantially Equivalent, May 29, 2019 |
| Received | Jan 31, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190167
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.