510(k) K080988 ยท DQY Catheter, Percutaneous
SCOUTPRO CS LEAD INTRODUCER SYSTEM
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, May 7, 2008 |
| Received | Apr 7, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080988
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.