510(k) K991775 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS
| Applicant | Mennen Medical, Inc., Rehovot, IL |
| Decision | Substantially Equivalent, Jun 24, 1999 |
| Received | May 25, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991775
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.