510(k) K770416 ยท DTB Permanent Pacemaker Electrode
LEAD, HEART, BUTTERFLY CLAMP
| Applicant | Arco Medical Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 10, 1977 |
| Received | Mar 4, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770416
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.