510(k) K810386 ยท DXY Implantable Pacemaker Pulse-Generator
THINLITH II PULSE GNEERATOR MODEL 227-05
| Applicant | Intermedics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 13, 1981 |
| Received | Feb 13, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810386
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.