510(k) K960849 ยท DTG Magnet, Test, Pacemaker
MAGNO ALARM
| Applicant | Cardiac Assist Devices, Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Mar 26, 1997 |
| Received | Feb 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960849
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.