510(k) K852340 ยท DXY Implantable Pacemaker Pulse-Generator
SUPRIMA MODEL 254-24
| Applicant | Intermedics, Inc., Freeport TX, US |
| Decision | Substantially Equivalent, Nov 8, 1985 |
| Received | Jun 3, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852340
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.