510(k) K903081 ยท DXY Implantable Pacemaker Pulse-Generator
NEOS (TM) 02 B PULSE GENERATOR
| Applicant | Biotronik, GmbH & Co., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Sep 14, 1990 |
| Received | Jul 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903081
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.