510(k) K033217 ยท DQY Catheter, Percutaneous
PHERON PTA CATHETER
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Oct 31, 2003 |
| Received | Oct 3, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033217
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.