510(k) K072200 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)
STIMLAB
| Applicant | Micropace Pty, Ltd., Canterbury, Nsw, AU |
| Decision | Substantially Equivalent, Oct 26, 2007 |
| Received | Aug 8, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072200
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.