510(k) K221397 ยท DRA Catheter, Steerable
MitraClip G4 Steerable Guide Catheter
| Applicant | ABBOTT MEDICAL, St.Paul MN, US |
| Decision | Substantially Equivalent, Sep 28, 2022 |
| Received | May 13, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221397
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.