510(k) K812932 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
ANERIOD GAUZE
| Applicant | Abco Dealers, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 2, 1981 |
| Received | Oct 20, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812932
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.