510(k) K792526 ยท DXY Implantable Pacemaker Pulse-Generator
PULSE GENERATOR, MODEL NO. LIT 222
| Applicant | Bentley Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 5, 1980 |
| Received | Dec 7, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792526
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.