510(k) K770478 ยท DTD Pacemaker Lead Adaptor
ADAPTER, CORDIS
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 30, 1977 |
| Received | Mar 11, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770478
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.