510(k) K123324 ยท DQY Catheter, Percutaneous
SELECTRA 7F CATHETERS
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jan 11, 2013 |
| Received | Oct 26, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123324
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.