510(k) K945627 ยท DXY Implantable Pacemaker Pulse-Generator
PIKOS LP 01, PIKOS LP E01
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Unknown, Mar 4, 1996 |
| Received | Nov 16, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945627
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.