510(k) K041574 ยท DTD Pacemaker Lead Adaptor
CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020
| Applicant | Guidant Corporation, St Paul MN, US |
| Decision | Substantially Equivalent, Jul 12, 2004 |
| Received | Jun 14, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041574
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.