510(k) K781327 ยท DTE Pulse-Generator, Pacemaker, External
PULSE GENERATOR, MODEL 240, EXTERNAL
| Applicant | Intermedics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 11, 1978 |
| Received | Aug 1, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781327
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.