510(k) K941937 ยท DXY Implantable Pacemaker Pulse-Generator
PIKOS E 01-B
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Unknown, Aug 30, 1994 |
| Received | Apr 21, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941937
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.