510(k) K862261 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Feb 19, 1987 |
| Received | Jun 13, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862261
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.