510(k) K092913 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)
EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04
| Applicant | Ep Medsystems, West Berlin NJ, US |
| Decision | Substantially Equivalent, Oct 16, 2009 |
| Received | Sep 22, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092913
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.