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 Diamond Medical with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 3, 1992: DMI BLOOD GAS ANALYZER/CARTRIDGE.
| Dec 3, 1992 | DMI BLOOD GAS ANALYZER/CARTRIDGEK924758 · CHL | 510(k) clearances |
| Jan 8, 1992 | DMI BLOD GAS ANALYZER/CARTRIDGEK915087 · CHL | 510(k) clearances |
| Feb 8, 1988 | DIAMOND MEDICAL, INC. MODEL DM 600K874710 · FFT | 510(k) clearances |
| Feb 8, 1988 | DIAMOND MEDICAL, INC. MODEL DM 800K874709 · FFT | 510(k) clearances |
| Feb 5, 1988 | MODEL ISO-2001 UNIV. PATIENT ISOLATION CIRCUITK875369 · FFT | 510(k) clearances |
| Mar 17, 1987 | DIAMOND MEDICAL, INC., MODEL DM 700K863298 · FFT | 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
