510(k) K905087 ยท DXY Implantable Pacemaker Pulse-Generator
TRIOS 02
| Applicant | Biotronik, GmbH & Co., Lake Oswego OR, US |
| Decision | Substantially Equivalent, May 7, 1991 |
| Received | Nov 13, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905087
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.