510(k) K833421 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)
PROGRAMMABLE STIMULATOR 2352
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Jan 30, 1984 |
| Received | Oct 3, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833421
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.