510(k) K791276 ยท DQX Wire, Guide, Catheter
PERVENOUS LEAD INTRODUCER SYSTEM
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 24, 1979 |
| Received | Jul 9, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791276
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.