510(k) K212026 ยท DQY Catheter, Percutaneous
Amplatzer Steerable Delivery Sheath
| Applicant | ABBOTT MEDICAL, Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 27, 2021 |
| Received | Jun 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212026
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 9, 2021 | Abbott Amplatzer Steerable Delivery Sheath Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.