Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Cardiovascular Devices with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 23, 1989: THE CDI(R) SYSTEM 400.
| May 23, 1989 | THE CDI(R) SYSTEM 400K890113 · DJY | 510(k) clearances |
| Jan 30, 1989 | CDI(R) 2000 BLOOD GAS MONITORK884228 · CBZ | 510(k) clearances |
| Jun 5, 1987 | CDI(TM) EXTRACORPOREAL BLOOD GAS SYSTEM 300K871221 · DRY | 510(k) clearances |
| Feb 19, 1987 | MODIFIED GAS-STAT(TM) MONITORING SYSTEMK864703 · DTY | 510(k) clearances |
| Jan 10, 1985 | INTRAVASCULAR BLOOD GAS SYSTEMK843912 · CCE | 510(k) clearances |
| Apr 17, 1984 | GAST STAT MONITORING SYSTEMK840749 · DTY | 510(k) clearances |
| May 27, 1983 | GAS-STAT MONITORING SYSTEMK831225 · DRY | 510(k) clearances |
| Dec 22, 1982 | EXTRACORPOREAL BLOOD GAS SYSTEMK822000 · DTY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
