510(k) K895110 ยท DTG Magnet, Test, Pacemaker
MAESTRO PACEMAKER TEST MAGNET
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent, Sep 26, 1989 |
| Received | Aug 15, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895110
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.