510(k) K911310 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
COROMETRICS 5566AAX NONINVASIVE BLOOD PRESSURE MOD
| Applicant | Ge Medical Systems Information Technologies, Wallingford CT, US |
| Decision | Substantially Equivalent, Jun 10, 1991 |
| Received | Mar 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911310
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 13, 2006 | Cordis Corporation Cordis INFINITI 6 French Diagnostic Catheter. Catalog 534-6xxT. That is:
534614T, 534615T, 534617T, 534618T, 534619T, 534620T, 534621T, 534622T, 534623T, 534624T, 534625T, 534627T, 534628T, 534629T, Terminated |
DQO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.