510(k) K831057 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
VIDEO-DILUTION TECH. MARK I INSTRUMENT
| Applicant | Angio Tec Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 19, 1983 |
| Received | Apr 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831057
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.