510(k) K911935 ยท DRR Amplifier And Signal Conditioner, Biopotential
CARDIAC ELECTROPHYSICAL LEAD SELECTOR, MODIFIED
| Applicant | Gould, Inc., Valley View OH, US |
| Decision | Substantially Equivalent, Jul 22, 1991 |
| Received | May 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911935
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.