510(k) K001180 ยท DTE Pulse-Generator, Pacemaker, External
TEMPORARY PACEMAKER EXTENSION CABLE, MODELS 5235, 5235A, 5235V, TEMPORARY PACEMAKER SURGICAL EXTENSION CABLE, MODELS 528
| Applicant | Pace Medical, Waltham MA, US |
| Decision | Substantially Equivalent, Jun 27, 2000 |
| Received | Apr 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001180
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.