510(k) K922218 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
IQ SYSTEM
| Applicant | Renaissance Technology, Inc., Newtown PA, US |
| Decision | Substantially Equivalent, Dec 8, 1992 |
| Received | May 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922218
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.