510(k) K820820 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
CARDIO REVUE CENTER
| Applicant | Diasonics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 29, 1982 |
| Received | Mar 24, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820820
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.