510(k) K222037 ยท DQY Catheter, Percutaneous
Selectra Lead Implantation System
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jul 19, 2022 |
| Received | Jul 11, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K222037
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.