510(k) K813153 ยท DTG Magnet, Test, Pacemaker
TEST MAGNET
| Applicant | Pacesetter Systems, Walker MI, US |
| Decision | Substantially Equivalent, Dec 2, 1981 |
| Received | Nov 6, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813153
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.