510(k) K875167 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
HORIZON 9000
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, May 31, 1988 |
| Received | Dec 16, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875167
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.