510(k) K111839 ยท DQY Catheter, Percutaneous
SELECTRA ACCESSORY KIT
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Sep 26, 2011 |
| Received | Jun 29, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111839
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.